Visualize Submit Comment

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	MIM:619093
Synonyms	DFNB116 [EXACT]
Parent Relationships	is_a autosomal recessive nonsyndromic deafness