autosomal recessive nonsyndromic deafness 119 Disease Ontology Browser

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Disease Ontology Browser

autosomal recessive nonsyndromic deafness 119 (DOID:0070673)
Alliance: disease page
Synonyms: DFNB119
Alt IDs: OMIM:619615
Definition: An autosomal recessive nonsyndromic deafness characterized by mild to profound sensorineural hearing loss that has_material_basis_in compound heterozygous mutation in the AFG2B gene on chromosome 15q21.

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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