autosomal dominant nonsyndromic deafness 51 Disease Ontology Browser

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Disease Ontology Browser

autosomal dominant nonsyndromic deafness 51 (DOID:0110577)
Alliance: disease page
Synonyms: autosomal dominant deafness 51; chromosome 9q21.11 duplication syndrome; DFNA51
Alt IDs: OMIM:613558, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the fourth decade of life with high frequency progressive hearing loss and has_material_basis_in a 269-kb duplication of chromosome 9q21.11 involving the TJP2 and FAM189A2 genes.

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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