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Summary Literature (0)
DOID:0110591 - autosomal dominant nonsyndromic deafness 7

Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by progressive high-tone hearing loss and has_material_basis_in variation in the chromosome region 1q21-q23.

Synonyms: autosomal dominant deafness 7, DFNA7

Xenbase Genes : lmx1a

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011074 - autosomal dominant nonsyndromic hearing loss 7


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant nonsyndromic deafness (is_a)