Term Name: autosomal recessive nonsyndromic deafness 117
Synonyms: autosomal recessive deafness 117, DFNB117
Definition: An autosomal recessive nonsyndromic deafness characterized by bilateral moderate-to-profound sensorineural deafness with onset in early childhood that has_material_basis_in homozygous mutation in the CLRN2 gene on chromosome 4p15.
Ontology: Human Disease [DOID:0070671]   ( DOID:0070671 )

Relationships
is a type of: autosomal recessive nonsyndromic deafness