Fetal and neonatal alloimmune thrombocytopenia

rare

A rare hematological disease characterized by maternal alloimmunisation against fetal platelet antigens that are inherited from the father and different from those present in the mother, and usually presents as a severe isolated thrombocytopenia in otherwise healthy newborns.

Identifiers: MONDO:0019415 Orphanet:853
Part of: Hemorrhagic disease Hereditary disease
Also known as: NAIT

Subtypes

All diseases Rare only

Disease	ID	Genes
Fetomaternal alloimmune thrombocytopenia 1	MONDO:0980723	ITGB3
Fetomaternal alloimmune thrombocytopenia 2	MONDO:0980724	ITGA2B
Fetomaternal alloimmune thrombocytopenia 3	MONDO:0980725	ITGA2

Rare disease

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