autosomal dominant nonsyndromic deafness 69 Disease Ontology Browser

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Disease Ontology Browser

autosomal dominant nonsyndromic deafness 69 (DOID:0110590)
Alliance: disease page
Synonyms: autosomal dominant deafness 69; DCUA; DFNA69; unilateral or asymmetric congenital deafness
Alt IDs: OMIM:616697, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the KITLG gene on chromosome 12q21.

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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