autosomal recessive nonsyndromic deafness 112 Disease Ontology Browser

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Disease Ontology Browser

autosomal recessive nonsyndromic deafness 112 (DOID:0111637)
Alliance: disease page
Synonyms: autosomal recessive deafness 112; DFNB112
Alt IDs: OMIM:618257
Definition: An autosomal recessive nonsyndromic deafness characterized by postlingual progressive sensorineural hearing impairment that has_material_basis_in homozygous or compound heterozygous mutation in the BDP1 gene on chromosome 5q13.2.

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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