Term Name: | autosomal recessive nonsyndromic deafness 116 |
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Synonyms: | DFNB116 |
Definition: | An autosomal recessive nonsyndromic deafness that has_material_basis_in homozygous or compound heterozygous mutation in the CLDN9 gene on chromosome 16p13.3. |
Ontology: | Human Disease [DOID:0112162] ( DOID:0112162 ) |