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Disease Ontology Browser
platelet-type bleeding disorder 8 (DOID:0060692)
Alliance: disease page
Synonyms: ADP platelet receptor P2Y12 defect; P2Y12 defect
Alt IDs: OMIM:609821, ICD10CM:D69.8, ORDO:36355
Definition: An inherited blood coagulation 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.

Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/05/2017
MGI 6.11
The Jackson Laboratory