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Disease Ontology Browser
autosomal dominant nonsyndromic deafness 89 (DOID:0070612)
Alliance: disease page
Synonyms: autosomal dominant deafness 89; DFNA89
Alt IDs: OMIM:620284
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the ATOH1 gene on chromosome 4q22.


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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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory