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Metadata
ID DOID:0112162
Name autosomal recessive nonsyndromic deafness 116
Definition An autosomal recessive nonsyndromic deafness that has_material_basis_in homozygous or compound heterozygous mutation in the CLDN9 gene on chromosome 16p13.3.
https://pubmed.ncbi.nlm.nih.gov/31175426/
Xrefs

OMIM:619093

Synonyms

DFNB116 [EXACT]

Parent Relationships

is_a autosomal recessive nonsyndromic deafness

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