Term Name: autosomal recessive nonsyndromic deafness 116
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 )

Relationships
is a type of: autosomal recessive nonsyndromic deafness