Hereditary thrombocytopenia with normal platelets

Orpha code: 268322OMIM code: 612004

Definicja

A rare, genetic, isolated constitutional thrombocytopenia disease characterized by decreased platelet counts, not associated with platelet morphology or function impairment, in multiple members of a family. Manifestations are variable, typically ranging from asymptomatic to mild bleeding diathesis (e.g. easy bruising, epistaxis, petechiae). Occasionally, a more severe bleeding tendency has been associated and a mild predisposition to infection and eczema has been reported.

Disease data
Klasyfikacja

Disease

Kod ORPHA
268322
Kod OMIM
612004
Kod ICD10
D69.4
Kod ICD11
-

No additional description.

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