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DOID:0110587 - autosomal dominant nonsyndromic deafness 66
Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the CD164 gene on chromosome 6q21.
Synonyms: DFNA66, autosomal dominant deafness 66,
Xenbase Genes :
MONDO:0014854 - autosomal dominant nonsyndromic hearing loss 66 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee