autosomal dominant nonsyndromic deafness 49 Disease Ontology Browser

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Disease Ontology Browser

autosomal dominant nonsyndromic deafness 49 (DOID:0110572)
Alliance: disease page
Synonyms: autosomal dominant deafness 49; DFNA49
Alt IDs: OMIM:608372, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized by moderate loss for low and mid frequencies and mild loss for high frequencies and has_material_basis_in variation in the chromosome region 1q21-q23.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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