Human genes for platelet-type bleeding disorder 8
Platelet-type bleeding disorder 8 [DOID:0060692]
A blood platelet disease characterized by mild to moderate mucocutaneous bleeding and absence of adenosine phosphate induced platelet aggregation that has_material_basis_in homozygous or compound heterozygous mutation in the P2RY12 gene on chromosome 3q.
Synonyms: platelet-type bleeding disorder 8, DOID:0060692, platelettype bleeding disorder 8, ADP platelet receptor P2Y12 defect, P2Y12 defect