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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: 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.

Disease References using Mouse Models (2)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory