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Disease Ontology Browser
MYH-9 related disease (DOID:0060651)
Alliance: disease page
Alt IDs: OMIM:153640, OMIM:153650, OMIM:155100, OMIM:605249, ICD10CM:D69.4, ORDO:182050
Definition: A blood platelet disease that has_material_basis_in mutations in the MYH9 gene. It is characterized by thrombocytopenia, enlarged platelets, sensorineural hearing loss and presenile cataract.

Disease References using Mouse Models (1)

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
10/10/2017
MGI 6.10
The Jackson Laboratory