|OBO ID: DOID:0111057|
|Term Name:||platelet-type bleeding disorder 11||Search Ontology:|
|Definition:||A blood platelet disease characterized by autosomal recessive inheritance of mild to moderate bleeding and defective platelet activation and aggregation in response to collagen that has_material_basis_in compound heterozygous mutation in the GP6 gene on chromosome 19q13. (2)|
|Ontology:||Human Disease (DOID:0111057)|
|is a type of:||
OTHER platelet-type bleeding disorder 11 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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