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Disease Ontology Browser
autosomal dominant nonsyndromic deafness 56 (DOID:0110581)
Alliance: disease page
Synonyms: autosomal dominant deafness 56; DFNA56
Alt IDs: OMIM:615629, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the TNC gene on chromosome 9q33.

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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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Send questions and comments to User Support. 		last database update
09/19/2023
MGI 6.22 		The Jackson Laboratory