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bn:01907311n
Noun Concept
Categories: Congenital defects of phagocyte number, function, or both, Autosomal dominant disorders, Enzyme defects, Autosomal recessive disorders, Rare diseases
EN
Kostmann syndrome  severe congenital neutropenia  Agranulocytosis infantilis hereditaria  congenital neutropenia  infantile genetic agranulocytosis
EN
Severe congenital neutropenia, also often known as Kostmann syndrome or disease, is a group of rare disorders that affect myelopoiesis, causing a congenital form of neutropenia, usually without other physical malformations. Wikipedia
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Sources
EN
Severe congenital neutropenia, also often known as Kostmann syndrome or disease, is a group of rare disorders that affect myelopoiesis, causing a congenital form of neutropenia, usually without other physical malformations. Wikipedia
Rare disorders Wikipedia Disambiguation
IS A
disease
rare disease
GENETIC ASSOCIATION
HAX1
HEALTH SPECIALTY
hematology
Wikipedia
EN
severe congenital neutropenia
Wikidata
EN
Kostmann syndrome
Wikipedia Redirections
EN
Agranulocytosis infantilis hereditaria, congenital neutropenia, infantile genetic agranulocytosis, Kostmann's disease, Kostmann disease, Kostmann syndrome

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