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DOID:0110589 - autosomal dominant nonsyndromic deafness 68
Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the HOMER2 gene on chromosome 15q25.
Synonyms: DFNA68, autosomal dominant deafness 68,
Xenbase Genes :
MONDO:0014740 - autosomal dominant nonsyndromic hearing loss 68 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee