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DO Term : MYH-9 related disease [DOID:0060651] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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.

synonyms:
155100,
OMIM:155100,
ORDO:182050,
ICD10CM:D69.4

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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