Term Name: autosomal recessive nonsyndromic deafness 3
Synonyms: autosomal recessive deafness 3, neurosensory nonsyndromic recessive deafness 3, DFNB3, NRSD3
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 MYO15A gene on chromosome 17p11.
Ontology: Human Disease [DOID:0110488]   ( DOID:0110488 )

Relationships
is a type of: autosomal recessive nonsyndromic deafness