autosomal recessive nonsyndromic deafness 116 Disease Ontology Browser

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Disease Ontology Browser

autosomal recessive nonsyndromic deafness 116 (DOID:0112162)
Alliance: disease page
Synonyms: DFNB116
Alt IDs: OMIM:619093
Definition: An autosomal recessive nonsyndromic deafness that has_material_basis_in homozygous or compound heterozygous mutation in the CLDN9 gene on chromosome 16p13.3.

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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