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ValueSet: Chronic Hematologic Diseases

Summary

Defining URL:https://www.napkon.de/fhir/ValueSet/chronic-hematologic-diseases-sct
Version:1.0.0
Name:ChronicHematologicDiseases
Title:Chronic Hematologic Diseases
Status:Active as of 2021-09-13
Definition:

Chronic hematologic diseases the context of pediatrics and COVID-19

Publisher:Charité - Universitätsmedizin Berlin
Source Resource:XML / JSON / Turtle

References

Logical Definition (CLD)

This value set includes codes based on the following rules:

 

Expansion

This value set has >1000 codes in it. In order to keep the publication size manageable, only a selection (1000 codes) of the whole set of codes is shown

Expansion based on SNOMED CT International edition 31-Jul 2021

All codes in this table are from the system http://snomed.info/sct

CodeDisplayDefinition
61261009Hemolytic anemia (disorder)
40108008Thalassemia (disorder)
127040003Sickle cell-hemoglobin SS disease (disorder)
62403005Glucose-6-phosphate dehydrogenase deficiency anemia (disorder)
87522002Iron deficiency anemia (disorder)
303011007:263502005=90734009Neutropenic disorder where Clinical course = Chronic
109995007Myelodysplastic syndrome (disorder)
64779008Blood coagulation disorder (disorder)
414022008Disorder of cellular component of blood (disorder)
183005Autoimmune pancytopenia
862001Anemia caused by chlorate (disorder)
934007Thalassemia intermedia
1963002Paroxysmal nocturnal hemoglobinuria
2694001Myelophthisic anemia
2835000Traumatic cardiac hemolytic anemia
2897005Thrombocytopenia due to immune destruction
2990008Lymphocytic leukemoid reaction
3239007Lymphocyte disorder
3272007Stomatocytosis
3571004Megaloblastic anemia due to pancreatic insufficiency
3902000Non dose-related drug-induced neutropenia
3947004High oxygen affinity hemoglobin polycythemia
3978000Hemolytic anemia due to warm antibody
4854004Acquired hemolytic anemia
4939006Hemolytic anemia due to nonlymphoid neoplasm
4984008Microcytic normochromic anemia
5300004Hemoglobin Bart's hydrops syndrome
5315003HNSHA due to increased adenosine deaminase activity
5430006Megaloblastic anemia due to hyperalimentation
5603006Autoimmune hemolytic anemia due to IgG
5876000Acquired pancytopenia
5967006A>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis
5994005Hereditary elliptocytosis due to deficiency of protein 4.1
6398009Idiopathic chronic cold agglutinin disease
6631009Thrombocytosis
6659005Megaloblastic anemia due to nontropical sprue
7391009Hemoglobin D trait
8214000Telangiectasia macularis eruptiva perstans
8857001Hereditary elliptocytosis due to alpha spectrin defect
9311003Hermansky-Pudlak syndrome
9417000Nucleotide storage pool disorder
9426002Erythrocytosis due to hydronephrosis
9434008Hereditary pyropoikilocytosis
9764001Anemia due to radiation
10205009Megaloblastic anemia due to exfoliative dermatitis
10294000Reactive mastocytosis
10564005Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
10619002Megaloblastic anemia due to poor nutrition
11376001Hereditary acanthocytosis
11491000Anemia due to niacin deficiency
11503009Relative anemia
11781007Autoimmune hemolytic anemia due to complement
12189000Coombs negative hemolytic anemia
12238007Megaloblastic anemia due to gastrectomy
12814002B lymphocyte disorder
12907000Thiamine-responsive megaloblastic anemia
13172003Chronic idiopathic thrombocytopenic purpura
14024008Humoral immunologic aplastic anemia
14087004Hereditary stomatocytosis
14126008Autosomal-linked pyridoxine refractory sideroblastic anemia
14333004Alloimmune neonatal neutropenia
14379009Dimorphic anemia
14514008Anemia due to disturbance of hemoglobin synthesis
15012007Granulocyte abnormality due to immune defect
15121005Hereditary elliptocytosis due to glycophorin C deficiency
15276008Drug-induced enzyme deficiency anemia
15326009beta^+^ Thalassemia, normal Hb A>2<, type 2
15332004Goats' milk anemia
15466007Erythrocytosis due to cerebellar hemangioma
16360009Delta-beta thalassemia
16402000Sickle cell trait
16427007Delta thalassemia
16645003Anemia caused by insect venom (disorder)
16964007Hereditary persistence of fetal hemoglobin thalassemia
17182001Agranulocytosis
17342003Hereditary pure erythrocytosis
17592003Platelet dysfunction due to aspirin
18273004Unstable hemoglobin disease
18323000Innocent bystander type hemolytic anemia
18637002Megaloblastic anemia of premature infant
18662002Acquired Heinz body anemia
19307009Drug-induced thrombocytopenic purpura
19442009Heterozygous thalassemia
19588001Erythrocytosis due to tissue hypoxemia
19636003Monocytosis
21043008Neutrophil cytomatrix disorder
21412009X chromosome-linked pyridoxine refractory sideroblastic anemia
21527007Chronic granulomatous disease, type IV
21914002Anemia of thyroid dysfunction
22098000Chronic idiopathic hemolytic anemia
22310002Chronic idiopathic monocytosis
22347002Anemia of gonadal dysfunction
22438006Anemia due to disturbance of proliferation AND/OR differentiation of hematopoietic stem cells
22716005Platelet disorder
22933009G-6-PD class I variant anemia
23205009Transient neonatal thrombocytopenia
23269001Double heterozygous sickling disorder
23371004Epsilon gamma delta beta thalassemia
24159007Persistent lymphocytosis
24620004Hemolytic anemia due to babesiosis
24661004G-6-PD class III variant anemia
24829000Eosinophilic ulcerative colitis
24962009Anemia due to vitamin E deficiency
24974008Myelokathexis
24975009Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
25065001Hemoglobin E disease
25251008HNSHA due to gamma glutamyl cysteine synthetase deficiency
25266006Hereditary spherocytosis due to spectrin deficiency
25443007X chromosome-linked pyridoxine responsive sideroblastic anemia
25472008Sickle cell-hemoglobin D disease
25502009Episodic lymphocytopenia
25601009Erythrocytosis due to autotransfusion
25881005Erythrocytosis due to low atmospheric pressure
26252007Chronic granulomatous disease, type IIA
26333003Megaloblastic anemia due to vitamin B>12< malabsorption with proteinuria
26409005Congenital dyserythropoietic anemia, type III
26682008Homozygous beta thalassemia
26848004Chorea acanthocytosis syndrome
26944003Acute megaloblastic anemia due to dialysis
27080008beta^0^ Thalassemia, deletion type
27342004Anemia of pregnancy
27366005Megaloblastic anemia due to hemodialysis
27798002Megaloblastic anemia due to impaired absorption of folate
28147001Hemolytic anemia due to Clostridium welchii
28319009Erythrocytosis due to cardiovascular disease
28975000Constitutional aplastic anemia
29120000Eosinophilic colitis
29177004Anemia due to pentose phosphate pathway defect
29272001Chronic granulomatous disease, type I
29551000Anemia due to oxygen
29789008Monocytic leukemoid reaction
30182008Thrombocytopenia due to extracorporeal circulation (disorder)
30418008Anemia of adrenal dysfunction
30575002Fanconi pancytopenia syndrome
30981000Secondary eosinophilia
31206006Refractory megaloblastic anemia
31820007Anemia of endocrine disorder
32092008Toxic neutropenia
32094009Megaloblastic anemia due to fish tapeworm
32117000Sulfhemoglobinemia
32648007Mild hereditary spherocytosis due to spectrin deficiency
32855007HPFH unlinked to beta-globulin gene cluster
32858009Hemolytic disease of fetus OR newborn due to ABO immunization
32942005Hereditary thromboasthenia
32984002Neonatal polycythemia
33183004Post infectious thrombocytopenic purpura
33491002Autoimmune hemolytic anemia due to IgA plus complement
33905008Hereditary spherocytosis due to deficiency of protein 4.2
34194007HNSHA due to pyrimidine-5'-nucleotidase deficiency
34247008Anemia due to mechanical damage
34395002Thrombocytopenia due to hypothermia
34397005Erythrocytosis due to uterine myoma
34629009Anemia due to zinc deficiency
34739009Urticaria pigmentosa, adult form
34852006G-6-PD class II variant anemia
34916006Neutrophil motility disorder
34925000Megaloblastic anemia due to inborn errors of metabolism
35434009Sickle cell-hemoglobin C disease
35703006Transient paroxysmal cold hemoglobinuria
35778001Megaloblastic anemia due to error of folate metabolism
36070007Wiskott-Aldrich syndrome
36467003Alpha plus thalassemia
36472007Hemoglobin S-F disease
36568005Hemolytic uremic syndrome of childhood
36617002Immediate hemolytic transfusion reaction
36874002Stress polycythemia
36919001Anemia due to lead
37272000Rh deficiency syndrome
37370005Megaloblastic anemia due to drugs
37465004Plasmacytosis
37492005Sex-linked thrombocytopenia
38064006Reactive monocytosis
38292009Red blood cell disorder
38589006Mixed hemoglobin disorder
38689004Hemolytic anemia due to infection
38697006Polycythemia due to donor twin transfusion
38911009Hereditary hemolytic anemia
38959009Methemoglobinemia
38970002Doan-Wright syndrome
39586009HPFH A gamma beta^+^ thalassemia
39778006Hemolytic transfusion reaction
40145002Congenital neutrophil actin dysfunction
40197009Chronic granulomatous disease, type IA
40387008Polyagglutinable erythrocyte syndrome
40679002Erythrocytosis due to alveolar hypoventilation
41387000HNSHA due to phosphofructokinase deficiency
41461004Platelet dysfunction due to drugs
41462006Anemia due to disturbance of proliferation AND/OR differentiation of erythroid precursor cells
41614006Hypoplastic anemia
41814009Neutropenia with dysgranulopoiesis
41841004Sideroblastic anemia
42461002Anemia due to copper
42484009HNSHA due to hexokinase deficiency
42601008Congenital hemolytic anemia
42616006Erythrocytosis due to hepatoma
42852008Infectious lymphocytosis
43346008Platelet procoagulant activity deficiency
43355006Eosinopenia
43707008Anemia due to heat
43858000Secondary aplastic anemia
43918003Erythrocytosis due to renal tumor
44206008Hapten type low affinity hemolytic anemia
44288006Anemia due to extrinsic red cell abnormality
44306006T lymphocyte disorder
44452003Normocytic hypochromic anemia
44456000Inappropriate secondary erythrocytosis
44641000HNSHA due to triosephosphate isomerase deficiency
44666001Microcytic hypochromic anemia
44865000Secondary polycythemia
44910003Megaloblastic anemia due to decreased intake of vitamin B>12<
44992005Failed attempted abortion with intravascular hemolysis
45098004Anemia due to multiple mechanisms
45828008Anemia in mother complicating pregnancy, childbirth AND/OR puerperium
46248003Hemoglobin E trait
46359005Neutropenia associated with infectious disease
46737006Normocytic normochromic anemia
46760003Estren-Dameshek anemia
47024008Sickle cell-hemoglobin E disease
47047009Thalassemia with other hemoglobinopathy
47084006beta^+^ Thalassemia, normal Hb A>2<, type 1, silent
47100003Anemia of prematurity
47144000Acute neutrophilia
47318007Drug-induced neutropenia
47516005Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
47526003HNSHA due to NADH diaphorase deficiency
47844003Megaloblastic anemia due to chronic hemolytic anemia
47986005Genetic anomaly of leukocyte
48250002Gaisbock's syndrome
48516007Acute infectious lymphocytosis
48553001Hemoglobin H disease
48580008Anemia due to starvation
48788004Cyclic thrombocytopenia
48813009Lymphocytopenia
48983004X chromosome-linked sideroblastic anemia
49227001Phosphatidylcholine-sterol acyltransferase deficiency
49284006Juvenile type megaloblastic anemia
49472006Megaloblastic anemia due to vitamin B>12< deficiency
49708008Anemia of chronic renal failure
49886003Thrombocytopenia due to blood loss
50220002Cellular immunologic aplastic anemia
50253007Secondary paroxysmal cold hemoglobinuria
50715003Pure red cell aplasia
50926003Job's syndrome
51053007Hemoglobin C disease
51071000Microangiopathic hemolytic anemia
51448009Platelet secretory disorder
51624005Dilutional thrombocytopenia
51667002Anemia due to riboflavin deficiency
51720005Gray platelet syndrome
52212006HNSHA due to glutathione reductase deficiency
52413004HNSHA due to glucose phosphate isomerase deficiency
52565000Non megaloblastic anemia associated with nutritional deficiency
52951008Congenital dyserythropoietic anemia
53165003Megaloblastic anemia
53743006Anemia following fetal blood loss
54006005Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder)
54097007White blood cell disorder
54569005Bernard Soulier syndrome
54698001Megaloblastic anemia due to Zollinger-Ellison syndrome
55444004Transient neonatal neutropenia
55907008Acquired aplastic anemia
55995005Hereditary spherocytosis
56205004HPFH nondeletion type
56478004Leukemoid reaction
56918001Dose-related drug-induced neutropenia
57020009Stokvis' disease
57160007Felty's syndrome
57192008Acute pure red cell aplasia
59106005Anemia due to decreased red cell production
59548005Congenital dyserythropoietic anemia, type I
59644002HNSHA due to phosphoglycerate kinase deficiency
60138009Anemia of pituitary deficiency
60164003Megaloblastic anemia due to blind loop syndrome
60504009Megaloblastic anemia due to congenital deficiency of intrinsic factor
60628003Mediterranean macrothrombocytopenia
60805002Hemolytic anemia with emphysema AND cutis laxa
61395005Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia
61744005Neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia
61777009Hemoglobin C-F disease
62074008Delta zero thalassemia (disorder)
62268000HNSHA due to diphosphoglycerate mutase deficiency
62389006Acute megaloblastic anemia due to severe illness
62609001Autoimmune hemolytic anemia due to IgG plus complement
62871001Idiopathic paroxysmal cold hemoglobinuria
63175003Localized extracutaneous mastocytosis
63444004Thrombocytopenia due to hypersplenism
63484008Drug-induced neutrophilia
63565007Congenital anemia
64249002Allergic eosinophilia
64936001Löffler's syndrome
65623009Immune neutropenia
65959000Beta thalassemia
66055002Alpha zero thalassemia
66262001Hereditary elliptocytosis due to beta spectrin-ankyrin interaction
66309005Antibody-mediated anemia
66612000Nutritional anemia
66729008Hemoglobin D disease
67023009Lymphocytosis
67894009Megaloblastic anemia due to increased requirements
68361004Late anemia due to isoimmunization
68700003Megaloblastic anemia due to error of cobalamin metabolism
68712004Lymphocytic hypoplasia
68870007Congenital dyserythropoietic anemia, type II
68913001Alpha thalassemia syndrome
69216008Hb Lepore thalassemia
69574002Anemia of parathyroid dysfunction
69981004Hereditary spherocytosis due to beta spectrin defect
70349007Pseudoneutrophilia
70958007Plasma cell hyperplasia of bone marrow
71436005Lazy leukocyte syndrome
71610005Neutrophilic leukemoid reaction
71692003Leukoerythroblastotic reaction
71716005Erythrocytosis due to renal cyst
71832003Autoimmune hemolytic anemia due to IgM
71855000Acute megaloblastic anemia secondary to total parenteral nutrition
71988008Aase syndrome
72272002Non malignant mast cell disease
72501006Anemia due to arsenic hydride
73073009Hereditary elliptocytosis due to beta spectrin defect in self-association
73162004Posttransfusion purpura
73190000epsilon gamma delta beta^0^ Thalassemia
73397007Heparin-induced thrombocytopenia
73891003Acute megaloblastic anemia due to nitrous oxide
74576004Acquired thrombocytopenia
74703006HNSHA due to pyruvate kinase deficiency
74789008Coombs positive hemolytic anemia
74912001Hemoglobin M disease
75063005Hemoglobinopathy with erythrocytosis
75331009Evans syndrome
75443009Hereditary elliptocytosis due to abnormal protein 4.1
75451007Thalassemia major
76050008Hemoglobin C trait
76243000Chronic granulomatous disease, type IVA
76336008Delta beta zero thalassemia
76366001Hemolytic anemia due to Bartonella
76621000Urticaria pigmentosa, infantile form
76762001Eosinophilic myopathy
76873001Polycythemia due to maternal-fetal transfusion
77084001Immunologic aplastic anemia
77330006Chronic granulomatous disease, type II
77358003Congenital leukocyte adherence deficiency
77413008Severe hereditary spherocytosis due to spectrin deficiency
77607006Drug-induced sideroblastic anemia
77663007Hemolytic anemia due to malaria
78129009Thrombotic thrombocytopenic purpura
78209002Hemolytic uremic syndrome, adult type
78345002Thrombocytopenia due to diminished platelet production
78378009Isoimmune neutropenia
78578005Erythrocytosis due to pulmonary disease
78677008Anemia due to pantothenic deficiency
78745000Urticaria pigmentosa
78908001HNSHA due to decreased adenosine deaminase activity
78997000Megaloblastic anemia due to vegetarianism
79035003Anemia due to unknown mechanism
79336007Familial eosinophilia
79592006Beta plus thalassemia
80126007Plummer-Vinson syndrome
80141007Hemoglobinopathy
80255009Maternal transfer neutropenia
80369006Chronic neutrophilia
80511004Erythrocytosis due to endocrine disorder (disorder)
80875006Achlorhydric anemia
80963002G-6-PD class V variant anemia
81711008Hemolytic anemia due to drugs
82003006G-6-PD class IV variant anemia
82190001Thrombocytopenia due to defective platelet production
82317007Chronic granulomatous disease, type III
82430007Acute megaloblastic anemia
82546001Reactive immunoproliferative disease
82835005Neonatal thrombocytopenia
82895008Megaloblastic anemia due to disease of small intestine
82980005Anemia of diabetes
83250000Delayed hemolytic transfusion reaction
83414005Macrocytic anemia
84027009Pernicious anemia
84188003Thalassemia syndrome
84260001Hemoglobinopathy with cyanosis
84828003Leukopenia
85422000alpha^+^ Thalassemia, nondeletion type
85557000HPFH deletion type
85559002Pelger-Huët anomaly
85570009Anemia due to vitamin A deficiency
85589009Radial aplasia-thrombocytopenia syndrome
85649008Megaloblastic anemia due to folate deficiency
85746008Anemia due to protein deficiency
86225009Hapten type high affinity hemolytic anemia
86242003alpha^+^ Thalassemia, deletion type
86325007Non megaloblastic anemia due to alcoholism
86448001Anemia due to vitamin B>6< deficiency
86635005Kasabach-Merritt syndrome
86715000Beta 0 thalassemia
86859003G-6-PD variant enzyme deficiency anemia
86986002Rh hemolytic disease of the newborn
87806008Megaloblastic anemia due to tropical sprue
87810006Megaloblastic anemia due to alcoholism
87902006Thrombocytopenia due to non-immune destruction
87994004Xerocytosis
88854002Chronic constitutional pure red cell aplasia
89454001Shwachman syndrome
89459006HPFH linked to beta-globulin gene cluster
89655007Congenital neutropenia
89810003^A^gamma delta beta^0^ thalassemia (disorder)
89962000Neonatal thrombocytopenia due to exchange transfusion
90175006Secondary acquired sideroblastic anemia
90414007Chronic acquired pure red cell aplasia
90501009Erythrocytosis due to defective oxygen transport
91217009Megaloblastic anemia due to pregnancy
91411007Autoimmune hemolytic anemia due to IgA
95416007Eosinophilia myalgia syndrome
95557003Red blood cell sequestration in liver
95605009HELLP syndrome
95624007Neonatal lymphocytopenia
95733001Eosinophilic keratitis
105599000Anemia related to disturbed DNA synthesis
105600002Disorder of neutrophils
105601003Quantitative disorder of neutrophils
105602005Quantitative abnormality of granulocytes
105603000Non-malignant lymphocyte AND/OR plasma cell disorder
109994006Essential thrombocythemia (clinical disorder)
109996008Refractory anemia (clinical)
109998009Refractory anemia with ringed sideroblasts (clinical)
110000005Refractory anemia with excess blasts in transformation (clinical)
111037009Basophilic hyperplasia
111396008Chediak-Higashi syndrome
111407006Hemolytic uremic syndrome
111469006Hemolytic disease of the newborn due to non-ABO, non-Rh isoimmunization
111570005Anemia due to infection
111571009Congenital atransferrinemia
111572002beta^0^ Thalassemia, nondeletion type
111574001Anemia due to copper deficiency
111575000Anemia due to membrane defect
111576004Acquired stomatocytosis
111577008Anemia due to enzyme deficiency
111578003Fructose 1,6-biphosphate aldolase A deficiency
111579006HNSHA due to glutathione synthetase deficiency
111581008Anemia due to physical agent
111583006Leukocytosis
111584000Reticular dysgenesis
111585004Neutropenia associated with autoimmune disease
111588002White clot syndrome
115963009Regenerative anemia
123767004Hemoglobinemia
123772008Homozygous hemoglobinopathy
123773003Heterozygous hemoglobinopathy
123777002Autoimmune leukopenia
124134002Deficiency of G-6PD
124188007Deficiency of glutathione reductase (NAD(P)H)
124297004Deficiency of hexokinase type IV
127034005Pancytopenia
127037003Toxic methemoglobinemia with cyanosis
127038008Hereditary hemoglobinopathy due to globin chain mutation
127039000Acquired hemoglobinopathy
127041004Sickle cell-beta-thalassemia
127042006Sickle cell beta plus thalassemia
127043001Sickle cell-beta^0^-thalassemia
127044007Sickle cell-delta beta^0^-thalassemia
127045008Sickle cell anemia with coexistent alpha-thalassemia
127046009Sickle cell trait with coexistent alpha-thalassemia
127047000Sickle cell-hemoglobin Lepore disease
127048005Sickle cell-Hemoglobin O Arab disease
127049002Primary (idiopathic) autoimmune hemolytic anemia
127050002Secondary autoimmune hemolytic anemia
127052005Secondary warm autoimmune hemolytic anemia
127053000Post-infectious cold agglutinin disease
127054006Cold agglutinin disease due to Epstein-Barr virus infection
127055007Chronic cold agglutinin disease
127056008Chronic cold agglutinin disease associated with B-cell neoplasm
127057004Paroxysmal cold hemoglobinuria
127058009Paroxysmal cold hemoglobinuria associated with tertiary syphilis
127060006Drug-induced immune hemolytic anemia, hapten type
127061005Autoimmune hemolytic anemia, categorized by antibody class AND/OR complement
127062003Erythrocytosis
127063008Erythrocytosis due to cyanotic congenital heart disease
127065001Familial erythrocytosis due to diphosphoglycerate mutase deficiency
127066000Familial polycythemia vera
127067009Stress neutrophilia
127218004Reactive follicular hyperplasia in the elderly
127319005Anemia due to alloimmune destruction of transfused red cells
128086004Hemolytic disorder
128090002Benign gestational thrombocytopenia
128091003Autoimmune thrombocytopenia
128092005Secondary autoimmune thrombocytopenia
128093000Alloimmune thrombocytopenia
128094006Alloimmune platelet transfusion refractoriness
128095007Acquired platelet function disorder
128096008Hereditary platelet function disorder
128098009Scott syndrome
128099001Platelet storage pool defect
128100009Mixed alpha granule and dense body deficiency
128101008Platelet factor V deficiency (factor V Quebec)
128102001Familial alpha>2< adrenergic receptor defect in platelets
128103006Isolated collagen aggregation defect
129638002Hemolytic anemia due to hyperbaric oxygen
129639005Hereditary neutrophilia
129640007Benign granulocytopenia in childhood
129641006Chronic benign neutropenia of childhood
129643009Chronic hypoplastic neutropenia
129644003Myeloperoxidase deficiency syndrome
129645002Adult G6PD deficiency of leukocytes syndrome
129654004Acquired PF-3 disease
154826009Secondary thrombocytopenia
165531008Lymphocytosis - absolute
189509003Refractory anemia without sideroblasts, so stated
190959006Hemophagocytic syndrome, infection-associated
190996002Severe combined immunodeficiency with reticular dysgenesis (disorder)
191128004Iron deficiency anemia due to dietary causes
191136008Idiopathic hypochromic anemia
191142007Vitamin B12 deficiency anemia due to malabsorption with proteinuria
191146005Congenital folate malabsorption anemia
191148006Folate deficiency anemia, drug-induced
191149003Folate deficiency anemia due to malabsorption
191150003Folate deficiency anemia due to liver disorders
191154007Combined B12 and folate deficiency anemia
191161006Vitamin C deficiency anemia
191169008Hereditary ovalocytosis
191170009Hemolytic anemia due to glutathione metabolism disorder
191172001Favism
191177007Hemolytic anemia due to hexokinase deficiency
191178002Hemolytic anemia due to pyruvate kinase deficiency
191179005Hemolytic anemia due to triose phosphate isomerase deficiency
191180008Anemia due to disorders of nucleotide metabolism
191187006Alpha trait thalassemia
191189009Beta thalassemia intermedia
191201002Hb F disease
191202009Hemoglobin Zurich disease
191210005Primary cold-type hemolytic anemia
191211009Primary warm-type hemolytic anemia
191212002Secondary cold-type hemolytic anemia
191213007Secondary warm-type hemolytic anemia
191216004Non-autoimmune hemolytic anemia
191217008Mechanical hemolytic anemia
191218003Toxic hemolytic anemia
191222008Hemoglobinuria due to hemolysis from external causes
191228007Acquired spherocytosis
191229004Pyknocytosis, infantile
191244003Aplastic anemia due to chronic disease
191246001Aplastic anemia due to infection
191247005Aplastic anemia due to radiation
191248000Aplastic anemia due to toxic cause
191251007Transient hypoplastic anemia
191255003Transient acquired pure red cell aplasia
191256002Idiopathic aplastic anemia
191260004Pyridoxine-responsive sideroblastic anemia
191261000Secondary sideroblastic anemia due to disease
191262007Secondary sideroblastic anemia due to drugs and toxins
191265009Anemia in neoplastic disease
191268006Chronic anemia
191273000Leukemoid reaction of the newborn
191322006Thrombocytopenia due to drugs
191323001Thrombocytopenia due to extracorporeal circulation of blood
191338000Primary splenic neutropenia
191345000Acquired neutropenia in newborn
191347008Cyclic hematopoiesis
191358004Hereditary eosinophilia
191360002Drug-induced eosinophilia
191372008Polycythemia due to cyanotic heart disease
191373003Polycythemia due to cyanotic respiratory disease
191388008Familial methemoglobinemia
191389000Idiopathic methemoglobinemia
191390009Drug-induced methemoglobinemia
198830009Intravascular hemolysis following abortive pregnancy
199244000Anemia during pregnancy - baby delivered
199245004Anemia in the puerperium - baby delivered during current episode of care
199246003Anemia during pregnancy - baby not yet delivered
199247007Anemia in the puerperium - baby delivered during previous episode of care
199248002Iron deficiency anemia of pregnancy
206434001Late anemia of newborn due to isoimmunization
206510008Transient neonatal thrombocytopenia due to exchange transfusion
206511007Transient neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia (disorder)
206512000Transient neonatal thrombocytopenia due to isoimmunization
233691007Asthmatic pulmonary eosinophilia
233692000Cryptogenic pulmonary eosinophilia
234338001Non-anemic red cell disorder
234339009Macrocytosis - no anemia
234340006Sideropenia
234341005Alcohol-related macrocytosis
234343008Normocytic anemia due to aplasia
234345001von Jaksch's anemia
234346000Dilutional anemia
234347009Anemia of chronic disease
234348004Anemia of renal disease
234349007Microcytic anemia
234350007Neonatal anemia
234352004Normocytic anemia due to chronic blood loss
234353009Congenital transferrin deficiency
234358000Megaloblastic anemia due to dietary causes
234360003Vegan's anemia
234361004Congenital deficiency of intrinsic factor
234362006Biermer's congenital pernicious anemia
234363001Imerslund-Grasbeck anemia
234364007Combined deficiency anemia
234365008Thiamine-responsive macrocytosis
234366009Alcohol-related sideroblastic anemia
234367000Pancytopenia with pancreatitis
234375006Transient erythroblastopenia of childhood
234376007Acquired red cell aplasia
234380002Kell isoimmunization of the newborn
234381003Maternal autoimmune hemolytic anemia
234383000Homozygous alpha thalassemia
234385007Alpha thalassemia-2 trait
234386008Hemoglobin Constant Spring trait
234387004Hemoglobin Lepore trait
234388009Delta-beta-Lepore thalassemia
234389001Alpha-beta thalassemia
234390005Gamma thalassemia
234391009Sickle cell anemia with high hemoglobin F
234392002Hemoglobin E/beta thalassemia disease
234393007Low affinity hemoglobin
234394001High affinity hemoglobin
234395000Congenital methemoglobinaema with defective methemoglobin-reducing system
234396004Congenital methemoglobinemia with abnormal methemoglobins
234400004Secondary polycythemia without excess erythropoietin
234401000Erythrocyte enzyme deficiency
234402007CNSHA - Chronic non-spherocytic hemolytic anemia
234403002PGK - Phosphoglycerokinase deficiency
234404008Glucose phosphate isomerase deficiency
234405009Triose phosphate isomerase deficiency
234407001Uridine monophosphate hydrolase deficiency
234408006Adenosine deaminase overproduction
234409003Erythrocyte membrane abnormality
234410008Hereditary elliptocytosis with transient poikilocytosis
234411007Blood group deletion syndrome
234412000Abnormal cation transport syndrome
234413005Alpha/beta lipoproteinemia
234414004Non-malignant white cell disorder
234416002X-linked hypogammaglobulinemia
234417006T-cell lymphocytosis
234418001Chronic benign granulocytopenia
234423001Chronic benign neutropenia
234424007Metabolic neutropenia
234425008Autoimmune neutropenia
234426009Corticosteroid-induced neutrophilia
234427000Monocytoid disorder
234428005Lymphocytoid disorder
234429002Chemotactic disorder
234431006Specific granule deficiency
234433009Myeloperoxidase deficiency
234434003Alder's anomaly
234435002Hereditary hypersegmentation
234436001Hemolytic erythrophagocytic syndrome
234437005Hemophagocytic lymphohistiocytosis
234469001Inherited platelet disorder
234470000Platelet membrane defect
234471001Glycoprotein Ia defect
234472008Glycoprotein Ib defect
234473003Platelet type von Willebrand's disease
234474009Dense body defect
234475005Thromboxane generation defect
234476006Cyclooxygenase deficiency
234477002Thromboxane synthetase deficiency
234478007Giant platelet syndrome
234479004Acquired platelet disorder
234482009Amegakaryocytic thrombocytopenia
234483004Megakaryocytic thrombocytopenia
234484005May-Hegglin anomaly
234485006Epstein syndrome
234486007Montreal syndrome
234487003Mediterranean thrombocytopenia
234500001Secondary thrombocytosis
234512002Post-splenectomy thrombocytosis
234513007Post-splenectomy leukocytosis
234576008Chronic familial neutropenia (disorder)
234582006Leukocyte adhesion deficiency - type 1
234583001LAD - Leukocyte adhesion deficiency type 2
234587000Neutrophil lactoferrin deficiency
234588005Neutrophil secondary granule deficiency
234589002Glutathione synthetase deficiency
234590006Gluthathione peroxidase deficiency
234591005Combined phagocytic defect
237617006Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness
237985009Pearson's syndrome
238091006Lecithin cholesterol acyltransferase deficiency
238092004Fish-eye disease
238931006Wells' syndrome
239910001Spanish toxic oil syndrome
240305000Neonatal thrombocytopenia due to platelet alloimmunization
240453002Oroya fever
240486003Parvoviral aplastic crisis
241954008Idiopathic anaphylaxis
247860002Familial benign neutropenia
248693006Chronic idiopathic neutropenia
267454002Acatalasemia
267513007Deficiency anemias
267517008Vitamin B12 deficiency anemia due to dietary causes
267518003Folate deficiency anemia due to dietary causes
267524009Constitutional aplastic anemia with malformation
267527002Aplastic anemia due to drugs
267530009Acute posthemorrhagic anemia
267532001Qualitative platelet disorder (disorder)
267534000Primary thrombocytopenia
267535004Congenital thrombocytopenic purpura
267540007Neutropenia due to irradiation
267550008Congenital methemoglobinemia
269175006Beta thalassemia trait
270117002Platelet type pseudo-von Willebrand disease
271737000Anemia
273985002Anemia due to isoimmunization
273986001Perinatal thrombocytopenia
275523003Pancytopenia-dysmelia
276268001T-cell mediated cytopenia
276448005Idiopathic sideroblastic anemia
276575001Autoimmune neonatal thrombocytopenia
276576000McIntosh syndrome
276578004Physiological anemia of infancy
276579007Late anemia of newborn
276580005Atypical isoimmunization of newborn
276628009Chloramphenicol-induced neutropenia
277543005Malignant white blood cell disorder
278363000Alcoholic macrocytosis
278484009Tropical pulmonary eosinophilia
285777008Idiopathic erythrocytosis
286928002Deficiency anemias, excluding iron
288327009Granulation anomaly
289317009Granulocyte granule deficiency
290246007Sideropenic anemia with reticuloendothelial siderosis
291262006Simple chronic anemia
294303000Acquired methemoglobinuria
295315008Acquired methemoglobinemia
296332004Acquired storage pool deficiency (platelets)
297307009Exhausted platelets
300980002Normocytic anemia
301317008Congenital nonspherocytic hemolytic anemia
302215000Thrombocytopenic disorder
302873008Thrombocytopenic purpura
303011007Neutropenic disorder
303060002Normocytic anemia following acute bleed
306058006Aplastic anemia
307333004Rhesus isoimmunization due to anti-D
307334005Rhesus isoimmunization due to anti-c
307335006Rhesus isoimmunization due to anti-E
307336007Rhesus isoimmunization due to anti-Cw
307337003Duffy isoimmunization of the newborn
307338008Kidd isoimmunization of the newborn
307342006Thrombocytopenia due to massive blood transfusion
307343001Acquired hemoglobin H disease
307592006Basophilic leukemia
307726001Anemia in ovarian carcinoma
309742004Drug-induced autoimmune hemolytic anemia
310647000Anemia secondary to renal failure
313291009Anemia during the puerperium
317226009Granulocytosis
319171004Qualitative abnormality of granulocyte
320150004Idiopathic eosinophilia
322096003Platelet sequestration
322699009Intracorpuscular hemolytic anemia
323079008Thrombocytopenia due to sequestration
323666000Anemia due to intrinsic red cell abnormality
350353007De Vaal's syndrome
351287008Reticular dysgenesis with congenital aleukocytosis
359531004Amegakaryocytic thrombocytopenia with congenital malformation
359536009Megakaryocytic aplasia
360495000Familial megaloblastic anemia
363041004Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism
367328005Secondary polycythemia with excess erythropoietin
367542003Eosinophilic asthma
370474006Eosinophilic myositis (disorder)
371046004Traumatic hemolytic anemia (disorder)
371074009Radiation thrombocytopenia (disorder)
371106008Idiopathic maternal thrombocytopenia (disorder)
371315009Iron deficiency anemia secondary to inadequate dietary iron intake (disorder)
373420004Upshaw-Schulman syndrome (disorder)
373421000Diarrhea-associated hemolytic uremic syndrome (disorder)
373422007Diarrhea-negative hemolytic uremic syndrome (disorder)
387702001Perinatal anemia (disorder)
387705004Hemolytic disease of fetus OR newborn due to isoimmunization (disorder)
387744007March hemoglobinuria (disorder)
387745008Sports anemia (disorder)
387759001Chronic granulomatous disease (disorder)
389147003Relative polycythemia (disorder)
389148008Pseudo-polycythemia (disorder)
389214003Diaphyseal dysplasia with anemia (disorder)
397007003Mast cell disorder (disorder)
397012002Cutaneous mastocytosis (disorder)
397013007Solitary cutaneous mastocytoma (disorder)
397014001Diffuse erythrodermic mastocytosis (disorder)
398250003Familial hemophagocytic lymphohistiocytosis (disorder)
398623004Refractory anemia with excess blasts (disorder)
398937006Cold autoimmune hemolytic anemia (disorder)
402404006Episodic angioedema with eosinophilia (disorder)
402653004Thrombocytopenic purpura due to defective platelet production (disorder)
402654005Thrombocytopenic purpura due to platelet consumption (disorder)
402793008Heritable disorder of neutrophil production (disorder)
402794002Heritable disorder of neutrophil function (disorder)
403735006Eosinophilia-myalgia syndrome from tryptophan (disorder)
403837005Wiskott-Aldrich autosomal dominant variant syndrome (disorder)
403838000Jung syndrome (disorder)
403839008Siccardi syndrome (disorder)
404170009Bullous urticaria pigmentosa (disorder)
404173006Familial mastocytosis (disorder)
406565005CD4 T lymphocyte deficiency (disorder)
406593009Methemoglobinemia due to nitrate poisoning
409089005Febrile neutropenia (disorder)
413532003Anemia due to blood loss (disorder)
413533008Anemia due to chronic blood loss (disorder)
413565006Aplastic anemia associated with metabolic alteration (disorder)
413566007Aplastic anemia associated with pancreatitis (disorder)
413567003Aplastic anemia associated with pregnancy (disorder)
413603009Autoimmune hemolytic anemia (disorder)
414023003Disorder of cellular component of blood in newborn (disorder)
414127000Erythrocytosis due to polycythemia vera (disorder)
414393003Hereditary disorder of cellular element of blood (disorder)
414394009Hereditary red blood cell disorder (disorder)
414395005Hereditary white blood cell disorder (disorder)
414850009Neutrocytosis
415005004Panleukopenia (disorder)
415283002Refractory anemia with excess blasts-1 (disorder)
415284008Refractory anemia with excess blasts-2 (disorder)
416180004Hemoglobin SS disease without crisis (disorder)
416214006Sickle cell-hemoglobin D disease without crisis (disorder)
416290001Hemoglobin S sickling disorder without crisis (disorder)
416417002Hereditary hemoglobin S (disorder)
416484003Sickle cell-hemoglobin E disease with crisis (disorder)
416638004Sickle cell-hemoglobin E disease without crisis (disorder)
416729007Neutropenia associated with AIDS
416826005Sickle cell-thalassemia disease with crisis (disorder)
416902009Uremic thrombocytopenia (disorder)
417048006Sickle cell-thalassemia disease without crisis (disorder)
417279003Hemoglobin S sickling disorder with crisis (disorder)
417357006Sickling disorder due to hemoglobin S (disorder)
417389002Disorder of basophils (disorder)
417425009Hemoglobin SS disease with crisis (disorder)
417517009Sickle cell-hemoglobin C disease with crisis (disorder)
417626001Thrombocytopenic purpura associated with metabolic disorder (disorder)
417672002Granulocytopenic disorder (disorder)
417683006Sickle cell-hemoglobin C disease without crisis (disorder)
417748003Sickle cell-hemoglobin D disease with crisis (disorder)
417967008Disorder of eosinophil (disorder)
419455006Disorder characterized by eosinophilia (disorder)
420543008Anemia associated with AIDS
421102007Aplastic anemia associated with AIDS
421132004Platelet dysfunction associated with uremia (disorder)
421312009Agranulocytosis associated with AIDS
421766003Thrombocytopenia associated with AIDS
421851008Acquired hemolytic anemia associated with AIDS
422167001Mycoplasmal anemia (disorder)
423486005Disseminated eosinophilic collagen disease (disorder)
424988008Anemia due to substance
426800001Febrile granulocytopenia (disorder)
427245000Febrile leukopenia (disorder)
427306008Hereditary hemoglobinopathy (disorder)
428383000Anemia due to medication
430478003Macrophage activation syndrome (disorder)
430822009Basophilic leukemoid reaction (disorder)
438476003Autoimmune thrombotic thrombocytopenic purpura (disorder)
438492008Hereditary thrombocytopenic disorder (disorder)
439007008Acquired thrombotic thrombocytopenic purpura (disorder)
440206000Hemoglobin SS disease with vasoocclusive crisis (disorder)
441134009Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type (disorder)
441322009Drug induced thrombotic thrombocytopenic purpura (disorder)
444108000Acute sickle cell splenic sequestration crisis (disorder)
444976001Congenital hemolytic uremic syndrome (disorder)
445542007Hemoglobin O-Arab trait (disorder)
447117006Hemoglobin H constant spring thalassemia (disorder)
449784008Diffuse infiltrative lymphocytosis syndrome (disorder)
462166006Fetal anemia
699208000Thrombocytopenia due to alcohol
703135009Anemia in malignant neoplastic disease (disorder)
703540008Majeed syndrome
707323002Anemia co-occurrent and due to chronic kidney disease
707324008Anemia in end stage renal disease
707480001Chronic hemolytic anemia (disorder)
709465004Periodontitis associated with Chediak-Higashi syndrome
709535007Periodontitis co-occurrent with infantile genetic agranulocytosis (disorder)
709608008Periodontitis associated with acquired neutropenia
710735009Periodontitis co-occurrent with leukocyte adhesion deficiency
710926008Periodontitis co-occurrent with familial neutropenia
710927004Periodontitis associated with cyclical neutropenia
711160007Eosinophil peroxidase deficiency (disorder)
711161006Hypochromic microcytic anemia with iron overload (disorder)
711407000Stormorken syndrome
712922002MYH9 related disease
713349004Anemia co-occurrent with human immunodeficiency virus infection (disorder)
713388002GATA 1 related cytopenia
713444005Hemophagocytic syndrome co-occurrent with human immunodeficiency virus infection (disorder)
713496008Anemia caused by zidovudine
713508003Aplastic anemia co-occurrent with human immunodeficiency virus infection (disorder)
713530002Agranulocytosis co-occurrent with human immunodeficiency virus infection
713533000Acquired hemolytic anemia co-occurrent with human immunodeficiency virus infection (disorder)
713694002Disorder of cellular component of blood caused by antiretroviral drug (disorder)
713910008Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent (disorder)
715342005Alpha thalassemia X-linked intellectual disability syndrome (disorder)
715526002Dehydrated hereditary stomatocytosis (disorder)
716192009Short stature and deafness with neutrophil dysfunction and facial dysmorphism syndrome (disorder)
716336002Congenital amegakaryocytic thrombocytopenia (disorder)
716682000Dominant beta-thalassemia (disorder)
717050005Autosomal recessive sideroblastic anemia (disorder)
717254007Familial pseudohyperkalemia (disorder)
717769007MYH9 macrothrombocytopenia syndrome (disorder)
717780007MBL - monoclonal B-cell lymphocytosis
717946000Megaloblastic anemia due to vitamin B12 deficiency secondary to intestinal disease (disorder)
717947009Vitamin B12 deficiency anemia caused by drug (disorder)
717948004Acquired iron deficiency anemia due to increased iron requirement (disorder)
718196002Beta thalassemia X-linked thrombocytopenia syndrome (disorder)
718553004White platelet syndrome (disorder)
718554005Medich giant platelet syndrome (disorder)
718614004Telangiectasia, erythrocytosis, monoclonal gammopathy, perinephric fluid collections and intrapulmonary shunting syndrome (disorder)
718716008Autoimmune hemolytic anemia mixed type (disorder)
718882006X-linked severe congenital neutropenia (disorder)
719019000WT limb blood syndrome (disorder)
719021005DK phocomelia syndrome (disorder)
719156006X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome (disorder)
719402008Lethal hemolytic anemia and genital anomaly syndrome (disorder)
719453009Congenital dyserythropoietic anemia type IV (disorder)
719816006X-linked sideroblastic anemia with spinocerebellar ataxia
720401009Cystic fibrosis with gastritis and megaloblastic anemia syndrome (disorder)
720465002Adult-onset autosomal recessive sideroblastic anemia (disorder)
720520009Attenuated Chédiak-Higashi syndrome (disorder)
720521008Autosomal dominant macrothrombocytopenia (disorder)
720950009Familial thrombocytosis (disorder)
720982007Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (disorder)
721184003Megaloblastic anemia due to folate deficiency due to increased requirement (disorder)
721185002Megaloblastic anemia due to folate deficiency in pregnancy and lactation (disorder)
721186001Megaloblastic anemia due to folate deficiency in prematurity (disorder)
721228006Huntington disease-like 2 (disorder)
721295000Acquired thiamine deficiency anemia (disorder)
721304007Refractory thrombocytopenia (disorder)
721882001Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome (disorder)
722005000Iron-refractory iron deficiency anemia (disorder)
722067005Severe combined immunodeficiency with hypereosinophilia (disorder)
722125003Overhydrated hereditary stomatocytosis (disorder)
722207000Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome (disorder)
722401001SFTS - Severe Fever with Thrombocytopenia Syndrome
722453009Cutaneous mastocytosis, short stature, hearing loss syndrome (disorder)
722475006X-linked congenital dyserythropoietic anemia with thrombocytopenia (disorder)
722585009Polycythemia neonatorum due to inherited disorder of erythropoietin production (disorder)
722586005Polycythemia neonatorum following blood transfusion (disorder)
722721004Familial hemolytic uremic syndrome (disorder)
722925004Transient neonatal neutropenia due to congenital viral infection
722926003Transient neonatal neutropenia due to neonatal bacterial sepsis (disorder)
723443003Neutrophil immunodeficiency syndrome (disorder)
723512008Revesz syndrome (disorder)
723623002Southeast Asian ovalocytosis (disorder)
724138007Mitochondrial myopathy with sideroblastic anemia syndrome (disorder)
724172004McLeod neuroacanthocytosis syndrome (disorder)
724556004Iron deficiency anemia due to blood loss (disorder)
724557008Acquired iron deficiency anemia due to decreased absorption (disorder)
724637001Isolated thrombocytopenia (disorder)
725034002Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)
725057008Nonspherocytic hemolytic anemia due to deficiency of adenosinetriphosphatase (disorder)
725105006Bleeding disorder due to deficiency of calcium and diacylglycerol-regulated guanine nucleotide exchange factor I (disorder)
725137007Neutropenia, monocytopenia, deafness syndrome (disorder)
725291001Defect of purinergic receptor p2y G protein-coupled 12 (disorder)
725463007Severe congenital hypochromic anemia with ringed sideroblasts (disorder)
726669007Central nervous system calcification, deafness, tubular acidosis, anemia syndrome (disorder)
732960002Secondary autoimmune hemolytic anemia co-occurrent and due to systemic lupus erythematosus
732962005Hemolytic anemia associated with chronic inflammatory disease
732963000Secondary autoimmune hemolytic anemia co-occurrent and due to lymphoproliferative disorder
732965007Secondary autoimmune hemolytic anemia co-occurrent and due to rheumatic disorder (disorder)
732966008Secondary autoimmune hemolytic anemia co-occurrent and due to ulcerative colitis (disorder)
733064004Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome
733096007Thyrocerebrorenal syndrome
734349003Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder)
735434003Acquired neutrophilia (disorder)
735435002Constitutional neutrophilia (disorder)
735436001Acquired disorder of neutrophil function (disorder)
735437005Disorder of neutrophil adhesion (disorder)
735438000Disorder of neutrophil chemotaxis (disorder)
735439008Constitutional eosinopenia (disorder)
735440005Acquired eosinopenia (disorder)
735442002Acquired eosinophilia (disorder)
735443007Acquired lymphocytopenia (disorder)
735444001Acquired lymphocytosis (disorder)
735452003Hereditary vitamin B12 deficiency anemia (disorder)
735453008Hereditary folate deficiency anemia (disorder)
735748002Neonatal hemolysis co-occurrent and due to systemic bacterial infection (disorder)
736024007Pancytopenia caused by medication (disorder)
737209002Neonatal polycythemia due to placental insufficiency
737210007Neonatal polycythemia due to intra-uterine growth retardation
737220002Metabolic anemia
737221003Congenital thrombocytopenia (disorder)
763713000Idiopathic CD4 lymphocytopenia (disorder)
763864008Persistent polyclonal B-cell lymphocytosis
765327005Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome
765748009Adult pure red cell aplasia (disorder)
765977002Bleeding disorder due to glycoprotein VI deficiency (disorder)
766982000Hemolytic anemia due to adenylate kinase deficiency (disorder)
767497003Congenital methemoglobinemia due to NADH-cytochrome b5 reductase 3 deficiency
767498008Autosomal recessive congenital methemoglobinemia type II (disorder)
767499000Autosomal recessive congenital methemoglobinemia type I
767657005Anemia due to and following chemotherapy
767658000Neutropenia due to and following chemotherapy
768556005Ataxia pancytopenia syndrome
769167005Vaso-occlusive pain co-occurrent and due to sickle cell disease (disorder)
770407006Chuvash polycythemia
770942003Severe congenital neutropenia type 3
770947009Autosomal dominant severe congenital neutropenia (disorder)
771075004Macrothrombocytopenia with mitral valve insufficiency
771511005Familial thrombocytosis with transverse limb defect
772126000Poikiloderma with neutropenia
773489008Hereditary cryohydrocytosis with normal stomatin (disorder)
774071007Trilineage bone marrow failure with developmental delay syndrome
774083009Neonatal autoimmune hemolytic anemia (disorder)
775909002Congenital neutropenia, myelofibrosis, nephromegaly syndrome (disorder)
778024005Monocyte-B natural killer dendritic cell deficiency syndrome
778027003Primary CD59 deficiency
778050009Idiopathic eosinophilic myositis (disorder)
782759001X-linked dyserythropoietic anemia with abnormal platelets and neutropenia (disorder)
782866008Eosinophilic peritonitis (disorder)
782880001Hemoglobinopathy Toms River (disorder)
782911008Hereditary cryohydrocytosis with reduced stomatin
782915004Acquired hemophagocytic lymphohistiocytosis associated with malignant disease (disorder)
782934004Bleeding diathesis due to collagen receptor defect
783058007Autosomal recessive severe congenital neutropenia due to glucose-6-phosphatase catalytic subunit 3 deficiency
414027002Disorder of hematopoietic structure (disorder)
652005Gangrenous tonsillitis
1518005Splenitis
1551001Osteomyelitis of femur (disorder)
1671000Sago spleen
2128005Disease of pharyngeal tonsil
3502005Cervical lymphadenitis
3542000Laceration extending into parenchyma of spleen with open wound into abdominal cavity
5256002Injury of spleen with open wound into abdominal cavity
5791006Cicatrix of adenoid
6461009Amygdalolith
6803002Salmonella osteomyelitis
7587000Acute osteomyelitis of shoulder region
8872002Osteomyelitis of pelvic region
10138007Bone marrow hyperplasia
10188004Acute osteomyelitis of hand
10345003Primary syphilis of tonsils
10351008Suppurative tonsillitis
10362008Accessory spleen
10893003Tuberculous adenitis
11461005Staphylococcal tonsillitis
13272007Masshoff's syndrome
13325005Chronic osteomyelitis of hand
14266003Atrophy of thymus gland
14465002Ulcerative tonsillitis
15170009Submandibular lymphadenitis
16294009Splenomegaly
16358007Chronic disease of tonsils AND/OR adenoids
16409009Tuberculosis of retroperitoneal lymph nodes
16485001Ulcer of tonsil
17028003Osteomyelitis of forearm
17363001Splenic sarcoidosis
17422006Ectopic thymic tissue
17604001Bilateral right-sidedness sequence
17741008Acute tonsillitis
19058002Congestive splenomegaly
19471005Lymphadenitis
19719003Benign lymphocytic infiltration of Jessner
19750001Pseudolymphoma
19956000Acute osteomyelitis of forearm
20213006Injury of spleen without open wound into abdominal cavity
20673009Disorder of thymus
20888002Neutrophilic hyperplasia of bone marrow
21120002Osteomyelitis of lower leg
21857006Glandular tularemia
22996003Splenic infarction
23023009Disorder of tonsil
23589004Injury of spleen
23761004Hyposplenism
23794001Paratracheal lymphadenopathy
23914009Ectopic splenic tissue
24181002Aplasia of thymus gland with immunodeficiency
24358005Accessory thymic tissue
24738006Osteomyelitis of petrous bone
27158007Injury of thymus gland
27254001Extramedullary hematopoiesis of spleen
27878001Follicular tonsillitis
28399005Tuberculosis of spleen
28769004Osteomyelitis of ankle AND/OR foot
30635002Abscess of thymus
31047003Lymphomatoid papulosis
32035007Chronic lymphadenitis
32392003Acute osteomyelitis of jaw
33261009Abscess of tonsil
34287003Sinus histiocytosis with massive lymphadenopathy
35082008Cervical thymic remnant
36585007Dermatopathic lymphadenitis
36752001Congenital splenomegaly
36760000Hepatosplenomegaly
37722001Ulceroglandular tularemia
38096003Functional asplenia
38297003Chronic osteomyelitis of jaw
38824008Congenital anomaly of the thymus
38831007Splenosis
39323002Hyperplasia of adenoids
40453004Hyperplasia of tonsils AND adenoids
40478000Cyst of thymus gland
40888008Congenital anomaly of the hematopoietic system
40970001Chronic osteomyelitis
41174002Acute adenitis
41582007Streptococcal tonsillitis
42780004Congenital lobulation of spleen
43325004Nontraumatic splenic rupture
43756009Traumatic rupture of spleen
43766001Fibrotic lymphadenopathy
44298000Lymph node abscess
44833003Pseudolymphoma of lung in Sjogren's disease
44897000Mesenteric lymphadenitis
46288008Payr's syndrome
46689006Hypertrophy of tonsils
48119005Dysplasia of thymus gland with immunodeficiency
48573006Suppurative lymphadenopathy
49498000Mesenteric adenitis due to Pasteurella multocida
49631001Acute mesenteric adenitis
49885004Hyperplasia of tonsils
50088001Hematoma of spleen without rupture of capsule AND without open wound into abdominal cavity
50797007Bubonic plague
51209006Viral tonsillitis
51244008Splenic disorder
51499002Disorder of tonsil and adenoid
52324001Mediastinal lymphadenopathy
52636001Actinic reticuloid
52967002Myelofibrosis
53453008Osteomyelitis of shoulder region
54084005Cervical tuberculous lymphadenitis
55366007Tonsillar tag
56118002Congenital syphilitic splenomegaly
56338005Splenic fibrosis
56517003Splenic hemorrhage
57375005Eosinophilic hyperplasia of bone marrow
57497006Congenital anomaly of spleen
58381000Hypersplenism
58639003Doan-Wiseman syndrome
58764007Tuberculous osteomyelitis
59867002Acute osteomyelitis of multiple sites
59934002Secondary syphilitic adenopathy
60168000Osteomyelitis
60684003SAPHO syndrome
61011009Bacterial osteomyelitis
61014001Laceration extending into parenchyma of spleen without open wound into abdominal cavity
61585002Osteomyelitis of hand
62042001Splenogonadal fusion
63375009Brodie's abscess
64757003Lymph node sarcoidosis
65146007Ectopic spleen
65875003Orbital osteomyelitis
66622006Hypertrophy of tonsils AND adenoids
66634003Chronic osteomyelitis of multiple sites
67322009Subacute osteomyelitis
67529001Cicatrix of tonsil
68164004Erythroid hyperplasia of bone marrow
70020005Adenoiditis
70529004Lymphoid hyperplasia of appendix
70918005Myeloid hyperplasia of bone marrow
72425000Bilateral left-sidedness sequence
73363000Oculoglandular tularemia
74387008Tuberculosis of hilar lymph nodes
75053002Acute febrile mucocutaneous lymph node syndrome
75286007Osteomyelitis of upper arm
75886002Sclerosing osteomyelitis of Garré
76616003Disorder of lymph node
77038006Tuberculosis of peripheral lymph nodes
78436002Tuberculosis of intrathoracic lymph nodes
79040006Splenic cyst
80192004Massive parenchymal disruption of spleen with open wound into abdominal cavity
80378000Neonatal hepatosplenomegaly
80507005Acute osteomyelitis of pelvic region
81339006Secondary syphilis of tonsil
82053000Splenic abscess
82495004Tuberculosis of mediastinal lymph nodes
82893001Splenic atrophy
83525004Megakaryocytic hyperplasia of bone marrow
83707009Neonatal osteomyelitis of jaw
84224006Suppurative osteomyelitis of jaw
85692003Tuberculosis of tracheobronchial lymph nodes
86006001Massive parenchymal disruption of spleen without open wound into abdominal cavity
87117006HIV infection with acute lymphadenitis
87415007Osteomyelitis of jaw
87500009Hilar lymphadenopathy
90176007Tonsillitis
90979004Chronic tonsillitis
91538002Osteomyelitis of multiple sites
91854005Acute leukemia in remission
91855006Acute leukemia
91856007Acute lymphoid leukemia in remission
91857003Acute lymphoid leukemia
91858008Acute monocytic leukemia in remission
91860005Acute myeloid leukemia in remission
91861009Acute myeloid leukemia
91918005Congenital absence of thymus
91964000Benign neoplasm of adenoid
91987008Benign neoplasm of axillary lymph nodes
92028001Benign neoplasm of lateral axillary lymph nodes
92032007Benign neoplasm of bronchopulmonary lymph nodes
92073008Benign neoplasm of cubital lymph nodes
92090002Benign neoplasm of epitrochlear lymph nodes
92104000Benign neoplasm of femoral lymph nodes
92135006Benign neoplasm of hypogastric lymph nodes
92141004Benign neoplasm of iliac lymph nodes
92143001Benign neoplasm of infraclavicular lymph nodes
92144007Benign neoplasm of inguinal lymph nodes
92149002Benign neoplasm of intercostal lymph nodes
92150002Benign neoplasm of intestinal lymph nodes
92152005Benign neoplasm of intra-abdominal lymph nodes
92155007Benign neoplasm of intrapelvic lymph nodes
92156008Benign neoplasm of intrathoracic lymph nodes
92184003Benign neoplasm of lingual tonsil
92197001Benign neoplasm of lymph node
92198006Benign neoplasm of lymph nodes of face
92199003Benign neoplasm of lymph nodes of head
92200000Benign neoplasm of lymph nodes of lower limb
92201001Benign neoplasm of lymph nodes of multiple sites
92202008Benign neoplasm of lymph nodes of neck
92203003Benign neoplasm of lymph nodes of upper limb
92213006Benign neoplasm of mediastinal lymph nodes
92215004Benign neoplasm of mesenteric lymph nodes
92251006Benign neoplasm of obturator lymph nodes
92254003Benign neoplasm of occipital lymph nodes
92263001Benign neoplasm of tonsil
92268005Benign neoplasm of paramammary lymph nodes
92269002Benign neoplasm of parametrial lymph nodes
92271002Benign neoplasm of pararectal lymph nodes
92274005Benign neoplasm of paravaginal lymph nodes
92280002Benign neoplasm of parotid lymph nodes
92282005Benign neoplasm of pectoral axillary lymph nodes
92299006Benign neoplasm of popliteal lymph nodes
92306009Benign neoplasm of preauricular lymph nodes
92324006Benign neoplasm of retroperitoneal lymph nodes
92325007Benign neoplasm of retropharyngeal lymph nodes
92333008Benign neoplasm of scalene lymph nodes
92408009Benign neoplasm of spleen
92414002Benign neoplasm of submandibular lymph nodes
92416000Benign neoplasm of submental lymph nodes
92417009Benign neoplasm of superficial inguinal lymph nodes
92419007Benign neoplasm of supraclavicular lymph nodes
92437008Benign neoplasm of thymus
92441007Benign neoplasm of tibial lymph nodes
92444004Benign neoplasm of tonsillar fossa
92447006Benign neoplasm of tracheobronchial lymph nodes
92487001Benign neoplasm of Waldeyer's ring
92501000Congenital cleft of thymus
92511007Burkitt's tumor of lymph nodes of axilla AND/OR upper limb
92512000Burkitt's tumor of lymph nodes of head, face AND/OR neck
92513005Burkitt's tumor of lymph nodes of inguinal region AND/OR lower limb
92524007Carcinoma in situ of adenoid
92642005Carcinoma in situ of lingual tonsil
92671006Carcinoma in situ of tonsil
92754004Carcinoma in situ of spleen
92770002Carcinoma in situ of tonsillar fossa
92803008Carcinoma in situ of Waldeyer's ring
92811003Chronic leukemia in remission
92812005Chronic leukemia
92813000Chronic lymphoid leukemia in remission
92814006Chronic lymphoid leukemia
92817004Chronic myeloid leukemia in remission
92818009Chronic myeloid leukemia
92946005Congenital abnormal shape of spleen
92953001Congenital abnormal shape of thymus
93030006Congenital absence of spleen
93049005Congenital cyst of spleen
93133006Letterer-Siwe disease of intra-abdominal lymph nodes
93134000Letterer-Siwe disease of intrapelvic lymph nodes
93135004Letterer-Siwe disease of intrathoracic lymph nodes
93136003Letterer-Siwe disease of lymph nodes of axilla AND/OR upper limb
93137007Letterer-Siwe disease of lymph nodes of head, face AND/OR neck
93138002Letterer-Siwe disease of lymph nodes of inguinal region AND/OR lower limb
93139005Letterer-Siwe disease of lymph nodes of multiple sites
93140007Letterer-Siwe disease of spleen
93142004Leukemia in remission
93143009Leukemia
93144003Leukemic reticuloendotheliosis of intra-abdominal lymph nodes
93145002Leukemic reticuloendotheliosis of intrapelvic lymph nodes
93146001Leukemic reticuloendotheliosis of intrathoracic lymph nodes
93150008Leukemic reticuloendotheliosis of lymph nodes of multiple sites
93151007Leukemic reticuloendotheliosis of spleen
93152000Leukemic reticuloendotheliosis of extranodal AND/OR solid organ site
93169003Lymphoid leukemia in remission
93182006Malignant histiocytosis of intra-abdominal lymph nodes
93183001Malignant histiocytosis of intrapelvic lymph nodes
93184007Malignant histiocytosis of intrathoracic lymph nodes
93185008Malignant histiocytosis of lymph nodes of axilla AND/OR upper limb
93186009Malignant histiocytosis of lymph nodes of head, face AND/OR neck
93187000Malignant histiocytosis of lymph nodes of inguinal region AND/OR lower limb
93188005Malignant histiocytosis of lymph nodes of multiple sites
93189002Malignant histiocytosis of spleen
93190006Malignant histiocytosis of extranodal AND/OR solid organ site
93191005Malignant lymphoma of intra-abdominal lymph nodes
93192003Malignant lymphoma of intrapelvic lymph nodes
93193008Malignant lymphoma of intrathoracic lymph nodes
93194002Malignant lymphoma of lymph nodes of axilla AND/OR upper limb
93195001Malignant lymphoma of lymph nodes of head, face AND/OR neck
93196000Malignant lymphoma of lymph nodes of inguinal region AND/OR lower limb
93197009Malignant lymphoma of lymph nodes of multiple sites
93198004Malignant lymphoma of spleen
93200005Malignant mast cell tumor of intra-abdominal lymph nodes
93201009Malignant mast cell tumor of intrapelvic lymph nodes
93202002Malignant mast cell tumor of intrathoracic lymph nodes
93203007Malignant mast cell tumor of lymph nodes of axilla AND/OR upper limb
93204001Malignant mast cell tumor of lymph nodes of head, face AND/OR neck
93205000Malignant mast cell tumor of lymph nodes of inguinal region AND/OR lower limb
93292008Congenital hypoplasia of spleen
93297002Congenital hypoplasia of thymus
93351001Congenital malposition of spleen
93361008Congenital malposition of thymus
93451002Di Guglielmo's disease
93472004Hemangioma of spleen
93477005Hemorrhage of thymus
93487009Hodgkin's disease, lymphocytic depletion of lymph nodes of axilla AND/OR upper limb
93488004Hodgkin's disease, lymphocytic depletion of lymph nodes of head, face AND/OR neck
93493001Hodgkin's disease, lymphocytic-histiocytic predominance of intra-abdominal lymph nodes
93494007Hodgkin's disease, lymphocytic-histiocytic predominance of intrapelvic lymph nodes
93495008Hodgkin's disease, lymphocytic-histiocytic predominance of intrathoracic lymph nodes
93496009Hodgkin's disease, lymphocytic-histiocytic predominance of lymph nodes of axilla AND/OR upper limb
93500006Hodgkin's disease, lymphocytic-histiocytic predominance of spleen
93505001Hodgkin's disease, mixed cellularity of lymph nodes of axilla AND/OR upper limb
93509007Hodgkin's disease, mixed cellularity of spleen
93514006Hodgkin's disease, nodular sclerosis of lymph nodes of axilla AND/OR upper limb
93518009Hodgkin's disease, nodular sclerosis of spleen
93520007Hodgkin's disease of intra-abdominal lymph nodes
93521006Hodgkin's disease of intrapelvic lymph nodes
93522004Hodgkin's disease of intrathoracic lymph nodes
93523009Hodgkin's disease of lymph nodes of axilla AND/OR upper limb
93524003Hodgkin's disease of lymph nodes of head, face AND/OR neck
93526001Hodgkin's disease of lymph nodes of multiple sites
93527005Hodgkin's disease of spleen
93530003Hodgkin's granuloma of intrapelvic lymph nodes
93531004Hodgkin's granuloma of intrathoracic lymph nodes
93532006Hodgkin's granuloma of lymph nodes of axilla AND/OR upper limb
93536009Hodgkin's granuloma of spleen
93541001Hodgkin's paragranuloma of lymph nodes of axilla AND/OR upper limb
93542008Hodgkin's paragranuloma of lymph nodes of head, face AND/OR neck
93543003Hodgkin's paragranuloma of lymph nodes of inguinal region AND/OR lower limb
93547002Hodgkin's sarcoma of intra-abdominal lymph nodes
93548007Hodgkin's sarcoma of intrapelvic lymph nodes
93549004Hodgkin's sarcoma of intrathoracic lymph nodes
93550004Hodgkin's sarcoma of lymph nodes of axilla AND/OR upper limb
93554008Hodgkin's sarcoma of spleen
93662008Primary malignant neoplasm of adenoid
93720005Primary malignant neoplasm of bone marrow
93868009Primary malignant neoplasm of lingual tonsil
94071006Primary malignant neoplasm of spleen
94096009Primary malignant neoplasm of thymus
94102002Primary malignant neoplasm of tonsillar fossa
94144008Primary malignant neoplasm of Waldeyer's ring
94148006Megakaryocytic leukemia in remission
94158005Secondary malignant neoplasm of adenoid
94181007Secondary malignant neoplasm of axillary lymph nodes
94217008Secondary malignant neoplasm of bone marrow
94227002Secondary malignant neoplasm of bronchopulmonary lymph nodes
94268006Secondary malignant neoplasm of cubital lymph nodes
94285008Secondary malignant neoplasm of epitrochlear lymph nodes
94299007Secondary malignant neoplasm of femoral lymph nodes
94330007Secondary malignant neoplasm of hypogastric lymph nodes
94336001Secondary malignant neoplasm of iliac lymph nodes
94338000Secondary malignant neoplasm of infraclavicular lymph nodes
94339008Secondary malignant neoplasm of inguinal lymph nodes
94344001Secondary malignant neoplasm of intercostal lymph nodes
94345000Secondary malignant neoplasm of intestinal lymph nodes
94347008Secondary malignant neoplasm of intra-abdominal lymph nodes
94350006Secondary malignant neoplasm of intrapelvic lymph nodes
94351005Secondary malignant neoplasm of intrathoracic lymph nodes
94379004Secondary malignant neoplasm of lingual tonsil
94392001Secondary malignant neoplasm of lymph node
94393006Secondary malignant neoplasm of lymph nodes of face
94394000Secondary malignant neoplasm of lymph nodes of head
94395004Secondary malignant neoplasm of lymph nodes of lower limb
94396003Secondary malignant neoplasm of lymph nodes of multiple sites
94397007Secondary malignant neoplasm of lymph nodes of neck
94398002Secondary malignant neoplasm of lymph nodes of upper limb
94408005Secondary malignant neoplasm of mediastinal lymph nodes
94410007Secondary malignant neoplasm of mesenteric lymph nodes
94446003Secondary malignant neoplasm of obturator lymph nodes
94449005Secondary malignant neoplasm of occipital lymph nodes
94458003Secondary malignant neoplasm of tonsil
94463004Secondary malignant neoplasm of paramammary lymph nodes
94464005Secondary malignant neoplasm of parametrial lymph nodes
94466007Secondary malignant neoplasm of pararectal lymph nodes
94469000Secondary malignant neoplasm of paravaginal lymph nodes
94475009Secondary malignant neoplasm of parotid lymph nodes
94477001Secondary malignant neoplasm of pectoral axillary lymph nodes
94494004Secondary malignant neoplasm of popliteal lymph nodes
94501001Secondary malignant neoplasm of preauricular lymph nodes
94519005Secondary malignant neoplasm of retroperitoneal lymph nodes
94520004Secondary malignant neoplasm of retropharyngeal lymph nodes
94528006Secondary malignant neoplasm of scalene lymph nodes
94603006Secondary malignant neoplasm of spleen
94609005Secondary malignant neoplasm of submandibular lymph nodes
94611001Secondary malignant neoplasm of submental lymph nodes
94612008Secondary malignant neoplasm of superficial inguinal lymph nodes
94614009Secondary malignant neoplasm of supraclavicular lymph nodes
94632009Secondary malignant neoplasm of thymus
94636007Secondary malignant neoplasm of tibial lymph nodes
94639000Secondary malignant neoplasm of tonsillar fossa
94642006Secondary malignant neoplasm of tracheobronchial lymph nodes
94682004Secondary malignant neoplasm of Waldeyer's ring
94686001Mixed cell type lymphosarcoma of intra-abdominal lymph nodes
94687005Mixed cell type lymphosarcoma of intrapelvic lymph nodes
94688000Mixed cell type lymphosarcoma of intrathoracic lymph nodes
94690004Mixed cell type lymphosarcoma of lymph nodes of head, face, and neck
94707004Mycosis fungoides of intra-abdominal lymph nodes
94708009Mycosis fungoides of intrapelvic lymph nodes
94709001Mycosis fungoides of intrathoracic lymph nodes
94710006Mycosis fungoides of lymph nodes of axilla AND/OR upper limb
94711005Mycosis fungoides of lymph nodes of head, face AND/OR neck
94714002Mycosis fungoides of spleen
94716000Myeloid leukemia in remission
94727003Neoplasm of uncertain behavior of adenoid
94908004Neoplasm of uncertain behavior of lingual tonsil
94921006Neoplasm of uncertain behavior of lymph node
94977008Neoplasm of uncertain behavior of tonsil
95111006Neoplasm of uncertain behavior of spleen
95136000Neoplasm of uncertain behavior of thymus
95142001Neoplasm of uncertain behavior of tonsillar fossa
95184009Neoplasm of uncertain behavior of Waldeyer's ring
95186006Nodular lymphoma of intra-abdominal lymph nodes
95187002Nodular lymphoma of intrapelvic lymph nodes
95188007Nodular lymphoma of intrathoracic lymph nodes
95192000Nodular lymphoma of lymph nodes of multiple sites
95193005Nodular lymphoma of spleen
95209008Plasma cell leukemia in remission
95210003Plasma cell leukemia
95224004Reticulosarcoma of intra-abdominal lymph nodes
95225003Reticulosarcoma of intrapelvic lymph nodes
95226002Reticulosarcoma of intrathoracic lymph nodes
95230004Reticulosarcoma of lymph nodes of multiple sites
95231000Reticulosarcoma of spleen
95260009Sézary's disease of lymph nodes of head, face AND/OR neck
95263006Sézary's disease of spleen
95423008Osteomyelitis of cranium
95424002Acute osteomyelitis of cranium
95425001Chronic osteomyelitis of cranium
95846001Red blood cell sequestration in spleen
109302008Diffuse sclerosing osteomyelitis
109303003Osteomyelitis of facial bone
109304009Osteomyelitis of frontal bone
109305005Osteomyelitis of zygomatic bone
109306006Osteomyelitis of sphenoid bone
109307002Osteomyelitis of temporal bone
109308007Osteomyelitis of nasal-orbital complex
109309004Acute osteomyelitis of facial bone
109310009Acute osteomyelitis of frontal bone
109311008Acute osteomyelitis of zygomatic bone
109312001Acute osteomyelitis of sphenoid bone
109313006Acute osteomyelitis of temporal bone
109314000Acute osteomyelitis of nasal-orbit complex
109316003Chronic osteomyelitis of frontal bone
109317007Chronic osteomyelitis of zygomatic bone
109318002Chronic osteomyelitis of sphenoid bone
109319005Chronic osteomyelitis of temporal bone
109320004Chronic osteomyelitis of nasal-orbit complex
109321000Garré's osteomyelitis of facial bones
109322007Garré's osteomyelitis of the frontal bone
109323002Garré's osteomyelitis of the zygomatic bone
109324008Garré's osteomyelitis of the sphenoid bone
109325009Garré's osteomyelitis of the temporal bone
109326005Garré's osteomyelitis of the nasal-orbit complex
109346000Osteoporotic bone marrow defect
109391009Kaposi's sarcoma of lymph nodes
109690000Garré's osteomyelitis of the maxilla
109691001Garré osteomyelitis of the mandible
109692008Osteomyelitis of maxilla
109693003Acute osteomyelitis of maxilla
109694009Chronic osteomyelitis of maxilla
109695005Osteomyelitis of mandible
109696006Acute osteomyelitis of mandible
109697002Chronic osteomyelitis of mandible
109953003Radiation injury of bone marrow
109991003Acute myelofibrosis (clinical)
109992005Vaquez's disease
109993000Chronic myeloproliferative disorder (clinical)
110002002Mast cell leukemia (clinical)
110004001Acute promyelocytic leukemia, FAB M3
110005000Acute myelomonocytic leukemia, FAB M4
110006004Prolymphocytic leukemia (clinical)
110007008Adult T-cell leukemia/lymphoma
110013004Overlapping malignant neoplasm of tonsil
110134008Simple laceration of tonsil
110135009Contaminated simple laceration of tonsil
110136005Complex laceration of tonsil
110137001Contaminated complex laceration of tonsil
110138006Avulsion of tonsil
110161008Abrasion of tonsil
110230006Burn of tonsillar area
110231005Burn erythema of tonsillar area
110232003Second degree burn of tonsillar area
110233008Third degree burn of tonsillar area
110260001Contusion of tonsil
111002006Proteinaceous lymphadenopathy
111590001Disorder of lymphoid system (disorder)
111591002Hypertrophy of adenoids
111684008Capsular tear without major disruption of parenchyma of spleen AND with open wound in abdominal cavity
111816002Pneumococcal tonsillitis
118612006Malignant histiocytosis (clinical)
118613001Hairy cell leukemia (clinical)
118615008Malignant mast cell tumor (clinical)
123616008Granulocytic hyperplasia of bone marrow
123617004Fleckmilz
123725008Mild bone marrow hyperplasia
123726009Moderate bone marrow hyperplasia
123727000Severe bone marrow hyperplasia
123728005Recurrent bone marrow hyperplasia
125574005Angiolymphoid hyperplasia with eosinophilia
126810008Neoplasm of tonsillar fossa
127035006Bone marrow disorder
127074004Superficial lymphadenopathy
127075003Deep lymphadenopathy
127076002Occipital lymphadenopathy
127077006Posterior auricular lymphadenopathy
127078001Anterior auricular lymphadenopathy
127079009Inferior auricular lymphadenopathy
127080007Parotid lymphadenopathy
127081006Facial lymphadenopathy
127082004Submandibular lymphadenopathy
127083009Submental lymphadenopathy
127084003Mandibular lymphadenopathy
127085002Submaxillary lymphadenopathy
127086001Cervical lymphadenopathy
127087005Lateral cervical lymphadenopathy
127088000Supraclavicular lymphadenopathy
127089008Jugular lymphadenopathy
127090004Anterior cervical lymphadenopathy
127091000Retropharyngeal lymphadenopathy
127092007Prelaryngeal lymphadenopathy
127093002Delphian lymphadenopathy
127094008Pretracheal lymphadenopathy
127095009Infraclavicular lymphadenopathy
127096005Scalene lymphadenopathy
127097001Thoracic lymphadenopathy
127098006Prevertebral lymphadenopathy
127099003Prepericardial lymphadenopathy
127100006Lateral pericardial lymphadenopathy
127101005Pulmonary lymphadenopathy
127103008Tracheobronchial lymphadenopathy
127104002Superior tracheobronchial lymphadenopathy
127105001Inferior tracheobronchial lymphadenopathy
127106000Tracheal lymphadenopathy
127107009Parasternal lymphadenopathy
127109007Anterior mediastinal lymphadenopathy
127110002Posterior mediastinal lymphadenopathy
127111003Esophageal lymphadenopathy
127112005Intercostal lymphadenopathy
127113000Diaphragmatic lymphadenopathy
127114006Innominate lymphadenopathy
127116008Gut-associated lymphadenopathy
127117004Celiac lymphadenopathy
127118009Superior mesenteric lymphadenopathy
127119001Juxtaintestinal lymphadenopathy
127120007Hepatic lymphadenopathy
127121006Cystic lymphadenopathy
127122004Lymphadenopathy of epiploic foramen
127123009Left gastric lymphadenopathy
127124003Lymphadenopathy of lesser curvature of stomach
127125002Lymphadenopathy of greater curvature of stomach
127126001Lymphadenopathy of lymph node ring of cardia of stomach
127127005Gastro-omental lymphadenopathy
127128000Pyloric lymphadenopathy
127129008Suprapyloric lymphadenopathy
127130003Subpyloric lymphadenopathy
127131004Retropyloric lymphadenopathy
127132006Pancreaticosplenic lymphadenopathy
127133001Splenic lymphadenopathy
127134007Pancreatic lymphadenopathy
127135008Pancreaticoduodenal lymphadenopathy
127136009Inferior pancreaticoduodenal lymphadenopathy
127137000Superior pancreaticoduodenal lymphadenopathy
127138005Inferior pancreatic lymphadenopathy
127139002Superior pancreatic lymphadenopathy
127140000Aortic lymphadenopathy
127141001Renal hilar lymphadenopathy
127142008Lumbar lymphadenopathy
127143003Intestinal lymphadenopathy
127144009Mesenteric lymphadenopathy
127145005Inferior mesenteric lymphadenopathy
127146006Sigmoid lymphadenopathy
127147002Superior rectal lymphadenopathy
127148007Ileocolic lymphadenopathy
127149004Right colic lymphadenopathy
127150004Midcolic lymphadenopathy
127151000Left colic lymphadenopathy
127152007Colic lymphadenopathy
127153002Common duct lymphadenopathy
127154008Retroperitoneal lymphadenopathy
127155009Prececal lymphadenopathy
127156005Retrocecal lymphadenopathy
127157001Appendicular lymphadenopathy
127158006Pelvic lymphadenopathy
127160008Medial common iliac lymphadenopathy
127161007Intermediate common iliac lymphadenopathy
127162000Lateral common iliac lymphadenopathy
127163005Subaortic common iliac lymphadenopathy
127164004Promontory lymphadenopathy
127166002External iliac lymphadenopathy
127167006Medial external iliac lymphadenopathy
127168001Intermediate external iliac lymphadenopathy
127169009Lateral external iliac lymphadenopathy
127170005Medial lacunar lymphadenopathy
127171009Interiliac lymphadenopathy
127172002Obturator lymphadenopathy
127173007Hypogastric lymphadenopathy
127174001Gluteal lymphadenopathy
127175000Inferior gluteal lymphadenopathy
127176004Superior gluteal lymphadenopathy
127177008Sacral lymphadenopathy
127178003Parametrial lymphadenopathy
127179006Epigastric lymphadenopathy
127180009Presymphysial lymphadenopathy
127181008Uterine paracervical lymphadenopathy
127182001Paravesicular lymphadenopathy
127183006Prevesicular lymphadenopathy
127184000Postvesicular lymphadenopathy
127185004Lateral vesicular lymphadenopathy
127186003Paravaginal lymphadenopathy
127187007Pararectal lymphadenopathy
127188002Upper extremity lymphadenopathy
127189005Axillary lymphadenopathy
127190001Lateral axillary lymphadenopathy
127191002Central axillary lymphadenopathy
127192009Apical axillary lymphadenopathy
127193004Pectoral axillary lymphadenopathy
127194005Subscapular axillary lymphadenopathy
127195006Paramammary lymphadenopathy
127196007Cubital lymphadenopathy
127197003Epitrochlear lymphadenopathy
127198008Lower extremity lymphadenopathy
127199000Inguinal lymphadenopathy
127200002Deep inguinal lymphadenopathy
127202005Superficial inguinal lymphadenopathy
127203000Superior medial inguinal lymphadenopathy
127204006Superior lateral inguinal lymphadenopathy
127205007Inferior inguinal lymphadenopathy
127206008Popliteal lymphadenopathy
127207004Deep popliteal lymphadenopathy
127208009Superficial popliteal lymphadenopathy
127209001Tibial lymphadenopathy
127210006Posterior tibial lymphadenopathy
127211005Anterior tibial lymphadenopathy
127212003Fibular lymphadenopathy
127213008Angiofollicular lymph node hyperplasia, hyaline-vascular type
127214002Angiofollicular lymph node hyperplasia, plasma cell type
127215001Progressively transformed germinal centers
127217009Histiocytic necrotizing lymphadenitis
127220001Malignant lymphoma of lymph nodes
127225006Chronic myelomonocytic leukemia
127226007Neoplasm of Waldeyer's ring
127227003Neoplasm of tonsil
127228008Neoplasm of adenoid
127229000Neoplasm of lingual tonsil
127230005Neoplasm of spleen
127231009Neoplasm of thymus
127232002Neoplasm of lymph node
127233007Neoplasm of lymph nodes of head
127234001Neoplasm of lymph nodes of face
127235000Neoplasm of lymph nodes of neck
127236004Neoplasm of occipital lymph nodes
127237008Neoplasm of parotid lymph nodes
127238003Neoplasm of preauricular lymph nodes
127239006Neoplasm of submandibular lymph nodes
127240008Neoplasm of submental lymph nodes
127241007Neoplasm of supraclavicular lymph nodes
127242000Neoplasm of retropharyngeal lymph nodes
127243005Neoplasm of infraclavicular lymph nodes
127244004Neoplasm of scalene lymph nodes
127245003Neoplasm of intrathoracic lymph nodes
127246002Neoplasm of bronchopulmonary lymph nodes
127247006Neoplasm of tracheobronchial lymph nodes
127248001Neoplasm of mediastinal lymph nodes
127249009Neoplasm of intercostal lymph nodes
127250009Neoplasm of intra-abdominal lymph nodes
127251008Neoplasm of intestinal lymph nodes
127252001Neoplasm of mesenteric lymph nodes
127253006Neoplasm of retroperitoneal lymph nodes
127254000Neoplasm of lymph nodes of upper limb
127255004Neoplasm of axillary lymph nodes
127256003Neoplasm of lateral axillary lymph nodes
127257007Neoplasm of pectoral axillary lymph nodes
127258002Neoplasm of paramammary lymph nodes
127259005Neoplasm of cubital lymph nodes
127260000Neoplasm of epitrochlear lymph nodes
127261001Neoplasm of lymph nodes of lower limb
127262008Neoplasm of inguinal lymph nodes
127263003Neoplasm of superficial inguinal lymph nodes
127264009Neoplasm of femoral lymph nodes
127265005Neoplasm of popliteal lymph nodes
127266006Neoplasm of tibial lymph nodes
127267002Neoplasm of intrapelvic lymph nodes
127268007Neoplasm of iliac lymph nodes
127269004Neoplasm of obturator lymph nodes
127270003Neoplasm of hypogastric lymph nodes
127271004Neoplasm of parametrial lymph nodes
127272006Neoplasm of paravaginal lymph nodes
127273001Neoplasm of pararectal lymph nodes
127274007Neoplasm of lymph nodes of multiple sites
128235003Abdominal lymphadenopathy
128862000Pseudolymphoma of Spiegler-Fendt
128864004Cutaneous T-cell pseudolymphoma
128865003Cutaneous B-cell pseudolymphoma
128873007Nodular scabies
129642004Chronic idiopathic immunoneutropenia in adult (disorder)
181225007Bilateral hilar adenopathy syndrome
186259007Scrofulous tuberculous abscess
186326007Pasteurella mesenteric adenitis
186792002Plasmodium vivax malaria with rupture of spleen
187084006Tonsillar aspergillosis
187694000Malignant tumor of adenoid
187716008Malignant tumor of Waldeyer's ring
187821001Angiosarcoma of spleen
187822008Fibrosarcoma of spleen
188489006Reticulosarcoma of lymph nodes of head, face and neck
188492005Reticulosarcoma of lymph nodes of axilla and upper limb
188493000Reticulosarcoma of lymph nodes of inguinal region and lower limb
188500005Lymphosarcoma of lymph nodes of head, face and neck
188501009Lymphosarcoma of intrathoracic lymph nodes
188502002Lymphosarcoma of intra-abdominal lymph nodes
188503007Lymphosarcoma of lymph nodes of axilla and upper limb
188504001Lymphosarcoma of lymph nodes of inguinal region and lower limb
188505000Lymphosarcoma of intrapelvic lymph nodes
188506004Lymphosarcoma of spleen
188507008Lymphosarcoma of lymph nodes of multiple sites
188511002Burkitt's lymphoma of intrathoracic lymph nodes
188512009Burkitt's lymphoma of intra-abdominal lymph nodes
188513004Burkitt's lymphoma of lymph nodes of axilla and upper limb
188514005Burkitt's lymphoma of lymph nodes of inguinal region and lower limb
188515006Burkitt's lymphoma of intrapelvic lymph nodes
188516007Burkitt's lymphoma of spleen
188517003Burkitt's lymphoma of lymph nodes of multiple sites
188524002Hodgkin's paragranuloma of intrathoracic lymph nodes
188529007Hodgkin's paragranuloma of intrapelvic lymph nodes
188531003Hodgkin's paragranuloma of lymph nodes of multiple sites
188536008Hodgkin's granuloma of intra-abdominal lymph nodes
188537004Hodgkin's granuloma of lymph nodes of axilla and upper limb
188538009Hodgkin's granuloma of lymph nodes of inguinal region and lower limb
188541000Hodgkin's granuloma of lymph nodes of multiple sites
188547001Hodgkin's sarcoma of lymph nodes of axilla and upper limb
188548006Hodgkin's sarcoma of lymph nodes of inguinal region and lower limb
188551004Hodgkin's sarcoma of lymph nodes of multiple sites
188554007Hodgkin's disease, lymphocytic-histiocytic predominance of lymph nodes of head, face and neck
188558005Hodgkin's disease, lymphocytic-histiocytic predominance of lymph nodes of axilla and upper limb
188559002Hodgkin's disease, lymphocytic-histiocytic predominance of lymph nodes of inguinal region and lower limb
188562004Hodgkin's disease, lymphocytic-histiocytic predominance of lymph nodes of multiple sites
188565002Hodgkin's disease, nodular sclerosis of lymph nodes of head, face and neck
188566001Hodgkin's disease, nodular sclerosis of intrathoracic lymph nodes
188567005Hodgkin's disease, nodular sclerosis of intra-abdominal lymph nodes
188568000Hodgkin's disease, nodular sclerosis of lymph nodes of axilla and upper limb
188569008Hodgkin's disease, nodular sclerosis of lymph nodes of inguinal region and lower limb
188570009Hodgkin's disease, nodular sclerosis of intrapelvic lymph nodes
188572001Hodgkin's disease, nodular sclerosis of lymph nodes of multiple sites
188575004Hodgkin's disease, mixed cellularity of lymph nodes of head, face and neck
188576003Hodgkin's disease, mixed cellularity of intrathoracic lymph nodes
188577007Hodgkin's disease, mixed cellularity of intra-abdominal lymph nodes
188578002Hodgkin's disease, mixed cellularity of lymph nodes of axilla and upper limb
188579005Hodgkin's disease, mixed cellularity of lymph nodes of inguinal region and lower limb
188580008Hodgkin's disease, mixed cellularity of intrapelvic lymph nodes
188582000Hodgkin's disease, mixed cellularity of lymph nodes of multiple sites
188585003Hodgkin's disease, lymphocytic depletion of lymph nodes of head, face and neck
188586002Hodgkin's disease, lymphocytic depletion of intrathoracic lymph nodes
188587006Hodgkin's disease, lymphocytic depletion of intra-abdominal lymph nodes
188589009Hodgkin's disease, lymphocytic depletion of lymph nodes of axilla and upper limb
188590000Hodgkin's disease, lymphocytic depletion of lymph nodes of inguinal region and lower limb
188591001Hodgkin's disease, lymphocytic depletion of intrapelvic lymph nodes
188592008Hodgkin's disease, lymphocytic depletion of spleen
188593003Hodgkin's disease, lymphocytic depletion of lymph nodes of multiple sites
188609000Nodular lymphoma of lymph nodes of head, face and neck
188612002Nodular lymphoma of lymph nodes of axilla and upper limb
188613007Nodular lymphoma of lymph nodes of inguinal region and lower limb
188627002Mycosis fungoides of lymph nodes of multiple sites
188631008Sezary's disease of intrathoracic lymph nodes
188632001Sezary's disease of intra-abdominal lymph nodes
188633006Sezary's disease of lymph nodes of axilla and upper limb
188634000Sezary's disease of lymph nodes of inguinal region and lower limb
188635004Sezary's disease of intrapelvic lymph nodes
188637007Sezary's disease of lymph nodes of multiple sites
188641006Malignant histiocytosis of lymph nodes of axilla and upper limb
188642004Malignant histiocytosis of lymph nodes of inguinal region and lower limb
188645002Leukemic reticuloendotheliosis of lymph nodes of head, face and neck
188648000Leukemic reticuloendotheliosis of lymph nodes of axilla and upper limb
188649008Leukemic reticuloendotheliosis of lymph nodes of inguinal region and lower limb
188662007Mast cell malignancy of lymph nodes of head, face and neck
188665009Mast cell malignancy of lymph nodes of axilla and upper limb
188666005Mast cell malignancy of lymph nodes of inguinal region and lower limb
188668006Mast cell malignancy of spleen
188669003Mast cell malignancy of lymph nodes of multiple sites
188725004Lymphoid leukemia
188726003Subacute lymphoid leukemia
188728002Aleukemic lymphoid leukemia
188729005Adult T-cell leukemia
188732008Myeloid leukemia
188733003Chronic eosinophilic leukemia
188734009Chronic neutrophilic leukemia
188736006Subacute myeloid leukemia
188737002Chloroma
188741003Aleukemic myeloid leukemia
188744006Histiocytic leukemia
188745007Chronic monocytic leukemia
188746008Subacute monocytic leukemia
188748009Aleukemic monocytic leukemia
188754005Thrombocytic leukemia
188768003Myelomonocytic leukemia
188770007Subacute myelomonocytic leukemia
190030009Compound leukemias
190995003Thymic aplasia or dysplasia with immunodeficiency
191377002Chronic mesenteric lymphadenitis
191382009Chronic congestive splenomegaly (disorder)
191384005Wandering spleen
191394000Calcified lymph nodes
195498006Lymph node fistula
195500007Lymph node infarction
195502004Lymph node rupture
195666007Acute erythematous tonsillitis
195667003Acute follicular tonsillitis
195668008Acute ulcerative tonsillitis
195669000Acute catarrhal tonsillitis
195670004Acute gangrenous tonsillitis
195671000Acute bacterial tonsillitis
195672007Acute pneumococcal tonsillitis
195673002Acute staphylococcal tonsillitis
195676005Acute viral tonsillitis
195677001Recurrent acute tonsillitis
195797002Adenoid vegetations
195798007Chronic adenotonsillitis
195803003Caseous tonsillitis
195804009Lingular tonsillitis
200697006Acute lymphadenitis of trunk
200698001Acute lymphadenitis of upper limb
200699009Acute lymphadenitis of lower limb
200700005Acute lymphadenitis of face, head and neck
203153007Acute osteomyelitis of lower leg
203157008Acute osteomyelitis-cervical spine
203158003Acute osteomyelitis-thoracic spine
203159006Acute osteomyelitis-lumbar spine
203160001Acute osteomyelitis-sacrum
203161002Acute osteomyelitis-coccyx
203162009Acute osteomyelitis-clavicle
203163004Acute osteomyelitis-scapula
203164005Acute osteomyelitis-humerus
203165006Acute osteomyelitis of radius
203166007Acute osteomyelitis of ulna (disorder)
203167003Acute osteomyelitis-carpal bone
203168008Acute osteomyelitis-metacarpal
203169000Acute osteomyelitis-phalanx of finger/thumb
203170004Acute osteomyelitis-femur
203171000Acute osteomyelitis-patella
203172007Acute osteomyelitis of tibia (disorder)
203173002Acute osteomyelitis of fibula (disorder)
203174008Acute osteomyelitis-calcaneum
203175009Acute osteomyelitis-talus
203177001Acute osteomyelitis-metatarsal
203178006Acute osteomyelitis-phalanx of toe
203179003Acute hematogenous osteomyelitis
203184009Chronic osteomyelitis of shoulder (disorder)
203185005Chronic osteomyelitis of upper arm
203186006Chronic osteomyelitis of radius and/or ulna
203189004Chronic osteomyelitis of lower leg (disorder)
203193005Chronic osteomyelitis-cervical spine
203194004Chronic osteomyelitis-thoracic spine
203195003Chronic osteomyelitis-lumbar spine
203196002Chronic osteomyelitis-sacrum
203197006Chronic osteomyelitis-coccyx
203198001Brodie's abscess of cervical spine
203199009Brodie's abscess of thoracic spine
203200007Brodie's abscess of lumbar spine
203201006Brodie's abscess of sacrum
203202004Brodie's abscess of coccyx
203221007Infection of coccyx
203222000Infection of clavicle
203241002Osteomyelitis of vertebra
203296008Subacute osteomyelitis of cervical spine
203297004Subacute osteomyelitis of thoracic spine
203298009Subacute osteomyelitis of lumbar spine
203299001Subacute osteomyelitis of sacrum
203300009Subacute osteomyelitis of coccyx
205735005Hypoplasia of spleen
205736006Mis-shapen spleen
207036003Angiofollicular lymph node hyperplasia
210089008Closed injury of thymus
210095009Open injury of thymus
210180009Closed injury of spleen
210188002Open injury of spleen
210190001Spleen injury with hematoma without rupture of capsule, with open wound into cavity
232371001Hemorrhage from adenoid bed
232417005Vincent's tonsillitis
232418000Acute infection of tonsillar remnant
232419008Enlargement of tonsil or adenoid
232420002Chronic adenoiditis
232422005Cryptic tonsil
232423000Tonsillar retention cyst
232424006Foreign body in tonsil
232425007Tonsillar hemorrhage
233743002Mediastinal lymph node sarcoidosis
233744008Hilar lymph node sarcoidosis
234088000Hyperplastic lymph node
234089008Hypoplastic lymph node
234090004Tuberculous mesenteric adenitis
234091000Atypical mycobacterial lymphadenitis
234092007Chronic bancroftian lymphadenitis
234093002Chronic Malayan filarial lymphadenitis
234094008Chronic Timorian filarial lymphadenitis
234501002Epidermoid cyst of spleen
234503004Hydatid cyst of spleen
234504005Polycystic spleen
234505006Splenic pseudocyst
234506007Fragmentation of spleen
234507003Subcapsular hematoma of spleen
234508008Delayed rupture of spleen
234509000Torsion of spleen
234510005Amyloidosis of spleen
234519006Bone marrow transplant rejection
234520000Failed bone marrow transplant engraftment
234522008Disease relapse in transplant marrow
236854007Septic splenitis
237656000Acute splenic tumor
238405002Acute cervical adenitis
238676008Lofgren's syndrome
240142002Acute osteomyelitis of foot (disorder)
240143007Ankle - acute osteomyelitis
240147008Chronic osteomyelitis of foot
240148003Ankle - chronic osteomyelitis
240149006Thigh - chronic osteomyelitis
240150006Pelvis - chronic osteomyelitis
240151005Chronic multifocal osteomyelitis
240152003Chronic osteomyelitis with draining sinus
240414006Cervical atypical mycobacterial lymphadenitis
240444009Fusobacterial necrotizing tonsillitis
240630008Hyperimmune malarious splenomegaly
240789006Hepatosplenic schistosomiasis
240793000Schistosomal splenomegaly
240794006Splenic schistosomal giant cell lymphoma
248488001Ulceration of lymph node
249423002Bleeding from tonsillar bed
254423005Carcinoma of lingual tonsil
262779007Hematoma of thymus
262780005Laceration of thymus
262818004Splenic hematoma
262819007Intraparenchymal hematoma of spleen
262820001Contusion of spleen
262821002Avulsion of spleen
262822009Laceration of spleen
262823004Capsular tear of spleen
262824005Transection of spleen
264508001Bilateral hilar adenopathy
264564001Red pulp hamartoma
266343004Tonsil and/or adenoid hypertrophy
267548000Nonspecific mesenteric adenitis
268017000Acute osteomyelitis of the ankle and foot
268019002Chronic osteomyelitis of ankle and/or foot (disorder)
268826001Spleen rupture due to birth trauma
269616004Secondary nodes - axilla/arm
271981000Tonsillar debris
362970003Disorder of hemostatic system
1286003Vitamin K deficiency coagulation disorder
1563006Protein S deficiency disease
1908008von Willebrand disease, type IIC
2036003Acquired factor VII deficiency disease
3230006Illegal abortion with afibrinogenemia
3760002Familial multiple factor deficiency syndrome, type V
4320005Factor V deficiency
6364000Acquired factor XIII deficiency disease
6647006Legal abortion with defibrination syndrome
6935003Familial hemorrhagic diathesis
7014009Mechanical purpura
7226007Infection-associated purpura
9489006Factor X inhibitor disorder
10153004Systemic fibrinogenolysis
10278007Factitious purpura
10934005Cryofibrinogenemia
12153008Acquired factor IX deficiency disease
12501008von Willebrand disease, type IIF
12546009Hemorrhagic disease of the newborn due to vitamin K deficiency
13507004Purpura fulminans
13993001Factor XIII inhibitor disorder
14230004Acquired factor VIII deficiency disease
15132005Acquired factor XII deficiency disease
16773005Drug-induced coagulation inhibitor disorder
16872008Severe hemophilia A
16922007Hereditary coagulation factor deficiency
18604004Factor XIII deficiency disease
19267009Lupus anticoagulant disorder
19520006von Willebrand disease, type IIB
20343006Pigmented purpuric lichenoid dermatitis of Gougerot and Blum
21112004Vascular hemostatic disease
21360006Spontaneous abortion with afibrinogenemia
24149006Hemorrhagic disease of the newborn due to factor II deficiency
24663001von Willebrand disease, type IIH
25904003Acquired coagulation factor deficiency
26029002Mild hemophilia A
26843008Antiphospholipid syndrome
27068000Failed attempted abortion with afibrinogenemia
27312002High molecular weight kininogen deficiency
28293008Hemophilia A
30479005Legal abortion with afibrinogenemia
31925001Hereditary factor I deficiency disease
32605001Transient neonatal disorder of coagulation
33169001Factor XI deficiency, type II
33297000Hereditary factor II deficiency disease
33344008Moderate hemophilia A
33820001Acquired factor X deficiency disease
34417008Disseminated intravascular coagulation in newborn
34478009Failed attempted abortion with defibrination syndrome
35066007von Willebrand disease, type IID
35554008Acquired factor XI deficiency disease
35913006Acquired factor V deficiency disease
36351005Antithrombin III deficiency
37193007Factor VII deficiency
37350004Hereditary factor X deficiency disease
38879000Factor XI inhibitor disorder
40855001Hereditary factor VII deficiency syndrome
41106001von Willebrand factor inhibitor disorder
41486008Eczematid-like purpura of Doucas and Kapetanakis
41690001Factor V inhibitor disorder
41788008Hemophilia B
41816006Secondary cryofibrinogenemia
43217004Hereditary factor XII deficiency disease
45366001Congenital dysfibrinogenemia
45963004Factor XI deficiency, type III
46981006Factor XII deficiency disease
47307007Factor VIII inhibitor disorder
48976006Prekallikrein deficiency
49177006Postpartum coagulation defect with hemorrhage
49762007Hereditary factor XI deficiency disease
50189006Hereditary factor XIII deficiency disease
50770000Spontaneous abortion with defibrination syndrome
52137009von Willebrand disease, type IIE
53751009Senile purpura
56231002Purpura annularis telangiectodes of Majocchi
58327003Factor I inhibitor disorder
61551003Familial multiple factor deficiency syndrome, type VI
61802005Primary cryofibrinogenemia
61810006Illegal abortion with defibrination syndrome
62410004Postpartum fibrinolysis with hemorrhage
62698000Defibrination syndrome following molar AND/OR ectopic pregnancy
64315007Familial multiple factor deficiency syndrome, type III
64509006Circulating anticoagulant disorder
65768009Familial multiple factor deficiency syndrome, type II
66909001Familial multiple factor deficiency syndrome, type IV
67406007Disseminated intravascular coagulation
69500007Blood coagulation disorder due to liver disease
71723006von Willebrand disease, type IIG
73975000Factor II deficiency
76407009Protein C deficiency disease
76642003Factor X deficiency
79674009Hyperheparinemia
80988005Mixed cryofibrinogenemia
81500003Steroid purpura
81783000Familial multiple factor deficiency syndrome
84048006Familial multiple factor deficiency syndrome, type I
85796009Afibrinogenemia following molar AND/OR ectopic pregnancy
86075001Coagulation factor deficiency syndrome
87397002von Willebrand disease, type IIA
88540000Factor XI deficiency, type I
88776002Hereditary factor V deficiency disease
89729000Factor IX inhibitor disorder
90935002Hemophilia
91304009Capillary fragility abnormality
95623001Neonatal coagulation disorder
95839005Disorder of fibrinolysis
95840007Hypoplasminogenemia
95841006Hereditary hypoplasminogenemia
95842004Autosomal dominant deficiency of plasminogen
95843009Acquired hypoplasminogenemia
95844003Dysplasminogenemia
95845002Hereditary dysplasminogenemia
105604006Deficiency of naturally occurring coagulation factor inhibitor
111199007Purpura pigmentosa chronica
111452009Postpartum afibrinogenemia with hemorrhage
111589005Dysfibrinogenemia
123786007Blood coagulation disorder with shortened coagulation time
123787003Blood coagulation disorder with prolonged coagulation time
123788008Blood coagulation disorder with shortened bleeding time
123789000Blood coagulation disorder with prolonged bleeding time
123790009Blood coagulation disorder with impaired clot retraction time
128088003Blood coagulation disorder, categorized by value of screening test
128105004von Willebrand disorder
128106003von Willebrand disease type 1
128107007von Willebrand disease type 2
128108002von Willebrand disease type 3
128113003von Willebrand disease type IB
128114009von Willebrand disease type IC
128115005Pseudo von Willebrand disease
154818001Congenital afibrinogenemia
180481005Anti-factor II disorder
181456001Antiprothrombin disorder
190809001Waldenstrom's hypergammaglobulinemic purpura
190810006Benign primary hypergammaglobulinemic purpura
190814002Cryoglobulinemic purpura
191287000Hemorrhagic disorder due to circulating anticoagulants
191288005Hemorrhagic disorder due to antithrombinemia
191289002Hemorrhagic disorder due to hyperheparinemia
191290006Hemorrhagic disorder due to increase in anti-8a
191291005Hemorrhagic disorder due to increase in anti-9a
191292003Hemorrhagic disorder due to increase in anti-10a
191293008Hemorrhagic disorder due to increase in anti-11a
191296000Deficiency of coagulation factor due to liver disease
191297009Deficiency of coagulation factor due to vitamin K deficiency
191298004Acquired factor II deficiency
200030007Postpartum coagulation defects - delivered with postnatal problem
200031006Postpartum coagulation defects with postnatal problem
206414002Perinatal purpura
234440005Factor VIII deficiency
234442002Hemophilia A with inhibitor
234444001Congenital factor IX deficiency variant
234445000Congenital factor IX deficiency with inhibitor
234446004Congenital von Willebrand's disease
234447008vWD - Congenital von Willebrand's disease type I
234448003Congenital von Willebrand's disease type II
234450006Congenital von Willebrand's disease type III
234451005Acquired von Willebrand's disease
234452003Contact factor deficiency
234453008Passovoy factor deficiency
234454002Prothrombin complex deficiency
234455001Fibrinogen abnormality
234456000Congenital fibrinogen abnormality
234457009Hypofibrinogenemia
234458004Hypodysfibrinogenemia
234459007Alpha chain defect dysfibrinogenemia
234460002Beta chain defect dysfibrinogenemia
234461003Gamma chain defect dysfibrinogenemia
234462005Acquired fibrinogen abnormality
234463000Combined coagulation factor deficiency
234464006Fibrinolytic bleeding syndrome
234465007Alpha-2-antiplasmin deficiency
234466008Acquired coagulation disorder
234467004Thrombophilia
234468009Heparin cofactor II deficiency
234493006Non-thrombocytopenic purpura
234494000Primary non-thrombocytopenic purpura
234495004Secondary non-thrombocytopenic purpura
234496003Metabolic purpura
234497007Embolic purpura
237336007Fibrinolysis - postpartum
237337003Afibrinogenemia - postpartum
238781005Itching purpura
238783008Familial pigmented purpuric eruption
238787009Secondary cutaneous vasculitis
239892009Primary antiphospholipid syndrome
239894005Primary antiphospholipid syndrome with multisystem involvement
239895006Secondary antiphospholipid syndrome
239897003Secondary antiphospholipid syndrome with multisystem involvement
267272006Postpartum coagulation defects
275446004Gardner-Diamond syndrome
277791008Purpura simplex
278365007Anticoagulant-induced bleeding
278366008Anticoagulant excess without bleeding
278504009Afibrinogenemia
282707003Acquired inhibitor of coagulation
284078000Purpuric rash
307091009Factor V Leiden mutation
307115002Homozygous Factor V Leiden mutation
307116001Heterozygous Factor V Leiden mutation
307514008Idiopathic factor VIII deficiency
307515009Autoimmune factor VIII deficiency
307517001Pregnancy-related factor VIII deficiency
307518006Malignancy-related factor VIII deficiency
359700009Hereditary von Willebrand disease type IA
359704000von Willebrand disease, type 1^a^
359709005von Willebrand disease type IA
359711001Hereditary von Willebrand disease type 2A
359714009von Willebrand disease type 2A
359717002Hereditary von Willebrand disease type 2B
359721009von Willebrand disease type 2B
359723007Acquired hypofibrinogenemia
359725000Hereditary von Willebrand disease type 2M
359727008Fibrinogen deficiency
359730001Acquired afibrinogenemia
359732009von Willebrand disease type 2N
361209006Dermite ocre of Favre
361210001Gravitational purpura
387778001Purpuric disorder (disorder)
402589000Contact purpura (disorder)
402848007Clothing purpura (disorder)
402849004Purpura due to increased intravascular pressure (disorder)
402850004Purpura due to prolonged vomiting and/or coughing (disorder)
402851000Neonatal purpura fulminans (homozygous protein C deficiency) (disorder)
402852007Hyperglobulinemic purpura (disorder)
402853002Cryofibrinogenemic purpura (disorder)
402854008Dysproteinemic purpura (disorder)
402865003Systemic lupus erythematosus-associated antiphospholipid syndrome (disorder)
403393000Stellate pseudoscar in senile purpura (disorder)
421527008Resistance to activated protein C due to Factor V Leiden
425949001Mild hemophilia A with inhibitor
426199009Congenital factor IX deficiency without inhibitor (disorder)
438360006Hereditary factor VIII deficiency disease without inhibitor (disorder)
438372000Hereditary factor IX deficiency disease with inhibitor (disorder)
438373005Severe hereditary factor VIII deficiency disease with inhibitor (disorder)
438599002Moderate hereditary factor VIII deficiency disease with inhibitor (disorder)
438792009Hereditary factor IX deficiency disease without inhibitor (disorder)
438827002Hereditary thrombophilic dysfibrinogenemia (disorder)
439000005Hyperfibrinogenemia (disorder)
439001009Acquired thrombophilia (disorder)
439002002Thrombophilia due to acquired protein C deficiency (disorder)
439006004Hereditary hyperhomocysteinemia (disorder)
439125003Thrombophilia due to acquired protein S deficiency (disorder)
439126002Thrombophilia due to acquired antithrombin III deficiency (disorder)
439145006Congenital hypofibrinogenemia (disorder)
439156006Acquired combined coagulation factor deficiency (disorder)
439157002Hereditary combined coagulation factor deficiency (disorder)
439274008Hereditary protein C deficiency (disorder)
439455002Hereditary factor XIII A subunit deficiency (disorder)
439458000Factor I deficiency disease (disorder)
439459008Hereditary factor XIII B subunit deficiency (disorder)
439460003Hereditary factor XIII A subunit and B subunit deficiency (disorder)
439698008Hereditary thrombophilia (disorder)
439699000Hereditary antithrombin III deficiency (disorder)
439701000Hereditary heparin cofactor II deficiency (disorder)
439702007Hereditary protein S deficiency (disorder)
439725008A disintegrin and metalloproteinase with thrombospondin type 1 motif 13 deficiency (disorder)
440820004Mild hereditary factor VIII deficiency disease without inhibitor (disorder)
440866009Severe hereditary factor IX deficiency disease with inhibitor (disorder)
440867000Moderate hereditary factor IX deficiency disease with inhibitor (disorder)
440868005Mild hereditary factor IX deficiency disease with inhibitor (disorder)
440924009Hereditary hyperfibrinogenemia (disorder)
440988005Heterozygous protein S deficiency (disorder)
440989002Prothrombin G20210A mutation (disorder)
440993008Severe hereditary factor VIII deficiency disease without inhibitor (disorder)
441001005Hereditary elevated factor XI (disorder)
441006000Moderate hereditary factor VIII deficiency disease without inhibitor (disorder)
441042008Hereditary elevated factor VIII (disorder)
441079006Thrombophilia due to antiphospholipid antibody (disorder)
441101007Heterozygous protein C deficiency (disorder)
441188004Homozygous protein C deficiency (disorder)
441189007Homozygous protein S deficiency (disorder)
441190003Severe hereditary factor IX deficiency disease without inhibitor (disorder)
441191004Moderate hereditary factor IX deficiency disease without inhibitor (disorder)
441192006Mild hereditary factor IX deficiency disease without inhibitor (disorder)
441420000Homozygous prothrombin G20210A mutation (disorder)
441421001Heterozygous prothrombin G20210A mutation (disorder)
441697004Gestational thrombophilia
441762006Thrombophilia due to immobilization
441945008Thrombophilia due to trauma (disorder)
441946009Thrombophilia due to myeloproliferative disorder
441990004Thrombophilia due to paroxysmal nocturnal hemoglobinuria
442078001Thrombophilia due to malignant neoplasm
442121006Thrombophilia due to vascular anomaly
442197003Thrombophilia due to drug therapy
442363001Thrombophilia due to vascular device
442654007Thrombophilia due to hormone therapy
442760001Thrombophilia due to antineoplastic agent therapy
609329007Asherson's syndrome
609456005Termination of pregnancy complicated by afibrinogenemia
609462000Termination of pregnancy complicated by defibrination syndrome
715559004Combined deficiency of factor V and factor VIII (disorder)
716746003Congenital alpha-2-antiplasmin deficiency (disorder)
717407006Congenital plasminogen activator inhibitor deficiency type 1 (disorder)
717935003Early onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn (disorder)
717936002Classic onset hemorrhagic disease of newborn due to vitamin K deficiency
717937006Late onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn (disorder)
723011009Acute purpuric eruption of skin (disorder)
724344004Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency (disorder)
724356003Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder)
724854007Purpura of skin and or skin-associated mucous membrane co-occurrent and due to coagulation disorder (disorder)
724855008Purpura of skin caused by mechanical force (disorder)
725157006Acquired purpura fulminans (disorder)
733028000Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome
737243006Purpura of skin co-occurrent and due to vascular fragility (disorder)
767712006Factor IX deficiency (disorder)
767713001Factor XI deficiency
773422002East Texas bleeding disorder (disorder)
774084003Neonatal antiphospholipid syndrome (disorder)
782909004Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
783142006Pancytopenia due to IKZF1 mutations
783194008Bleeding diathesis due to thromboxane synthesis deficiency
783250007Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
783251006Hereditary thrombocytopenia with normal platelets
783255002Hereditary isolated aplastic anemia
783256001Familial thrombomodulin anomalies (disorder)
785308008Acquired hemophilia
789291002Venom-induced consumption coagulopathy - VICC
789660001Atypical hemolytic uremic syndrome (disorder)
860725002Low von Willebrand factor
866152006Thrombocytopenia due to SARS-CoV-2
1148849001Fibrinolytic disorder caused by urokinase
1148857003Fibrinolytic disorder caused by tissue plasminogen activator
1148859000Drug-induced fibrinolytic disorder
1148862002Factor X deficiency due to systemic amyloidosis
1148929009Deficiency of coagulation factor due to vitamin K malabsorption
1148930004Deficiency of coagulation factor due to vitamin K malabsorption in obstructive biliary disease (disorder)
1156746003Vaccine-induced prothrombotic immune thrombocytopenia
1156838007X-linked thrombocytopenia with normal platelets (disorder)
39191000119103Disseminated intravascular coagulation due to placental abruption (disorder)
62751000119108Fetal hemophilia
72161000119100Antiphospholipid syndrome in pregnancy
97571000119109Thrombocytopenia co-occurrent and due to alcoholism (disorder)
118791000119106Aplastic anemia caused by antineoplastic agent
328301000119102Pancytopenia due to antineoplastic chemotherapy (disorder)
328371000119107Pancytopenia caused by antithyroid drug (disorder)
328381000119105Pancytopenia caused by anticonvulsant
10749581000119100Blood coagulation disorder complicating childbirth
10749641000119106Blood coagulation disorder in pregnancy
10752381000119101Fetal thrombocytopenia
16623961000119100Pancytopenia caused by immunosuppressant

Explanation of the columns that may appear on this page:

Level A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies
Source The source of the definition of the code (when the value set draws in codes defined elsewhere)
Code The code (used as the code in the resource instance)
Display The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application
Definition An explanation of the meaning of the concept
Comments Additional notes about how to use the code