autosomal recessive nonsyndromic deafness 117 Disease Ontology Browser

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Disease Ontology Browser

autosomal recessive nonsyndromic deafness 117 (DOID:0070671)
Alliance: disease page
Synonyms: DFNB117
Alt IDs: OMIM:619174
Definition: An autosomal recessive nonsyndromic deafness characterized by bilateral moderate-to-profound sensorineural deafness with onset in early childhood that has_material_basis_in homozygous mutation in the CLRN2 gene on chromosome 4p15.

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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