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Genetic / Hereditary

This dimension names the agent that actually causes a medical condition, a pathogen, a genetic mutation or an environmental factor. Wikipedia notes that "a disease may be caused by external factors such as pathogens or by internal dysfunctions." Browsing this way collects every condition caused by the same agent.

Facts

Comparison

ICD-10 Chapter Number

III 1

ICD-10 Code Range

D50-D89 1

Genetic / Hereditary

77 entries

Body System

ICD-10 Chapter

Communicable or Non-communicable

Transmission Route

Era (First Described)

Treated By

Discoverer

Prevalence Band

Adenosine deaminase 2 deficiency

Adenosine deaminase deficiency

Alpha-thalassemia

Antithrombin III Deficiency

Atypical hemolytic uremic syndrome

Autoimmune lymphoproliferative syndrome

Bare lymphocyte syndrome

Bare lymphocyte syndrome type II

Blau syndrome

CD25 deficiency

Chronic Granulomatous Disease

Chronic mucocutaneous candidiasis

Combined immunodeficiencies

Common Variable Immunodeficiency

Complement 2 deficiency

Complement 3 deficiency

Congenital amegakaryocytic thrombocytopenia

Congenital dyserythropoietic anemia

Cyclic neutropenia

Diamond-Blackfan anemia

DiGeorge Syndrome

DOCK8 deficiency

Emberger syndrome

Epstein syndrome

Factor V Leiden

Factor XII deficiency

Factor XIII deficiency

Fanconi anemia

Glucose-6-Phosphate Dehydrogenase Deficiency

Griscelli syndrome type 2

Harris platelet syndrome

Hemoglobin D

Hereditary elliptocytosis

Hereditary persistence of fetal hemoglobin

Hereditary pyropoikilocytosis

Hereditary Spherocytosis

Hereditary stomatocytosis

Hoyeraal-Hreidarsson syndrome

Hyper IgM syndrome

Hypogammaglobulinemia

Hypoprothrombinemia

Immunodeficiency-centromeric instability-facial anomalies syndrome

Isolated congenital asplenia

Janus kinase 3 deficiency

LIG4 syndrome

LPS-responsive beige-like anchor protein deficiency

May-Hegglin anomaly

McLeod syndrome

MonoMAC

Muckle-Wells syndrome