Term Name: autosomal recessive nonsyndromic deafness 29
Synonyms: autosomal recessive deafness 29, DFNB29
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the CLDN14 gene on chromosome 21q22.
Ontology: Human Disease [DOID:0110487]   ( DOID:0110487 )

Relationships
is a type of: autosomal recessive nonsyndromic deafness