Term Name: autosomal recessive nonsyndromic deafness 18A
Synonyms: autosomal recessive deafness 18A, DFNB18A
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 USH1C gene on chromosome 11p15.
Ontology: Human Disease [DOID:0110473]   ( DOID:0110473 )

Relationships
is a type of: autosomal recessive nonsyndromic deafness