autosomal recessive nonsyndromic deafness 1B Disease Ontology Browser

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Disease Ontology Browser

autosomal recessive nonsyndromic deafness 1B (DOID:0110476)
Alliance: disease page
Synonyms: autosomal recessive deafness 1B; DFNB1B
Alt IDs: OMIM:612645, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually stable hearing loss and has_material_basis_in mutation in the GJB6 gene on chromosome 13q12.

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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