Term Name: autosomal recessive nonsyndromic deafness 9
Synonyms: autosomal recessive deafness 9, DFNB9, neurosensory nonsyndromic recessive deafness 9, NRSD9
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually severe to profound, stable hearing loss and has_material_basis_in mutation in the OTOF gene on chromosome 2p23.
Ontology: Human Disease [DOID:0110535]   ( DOID:0110535 )

Relationships
is a type of: autosomal recessive nonsyndromic deafness