Term Name: autosomal recessive nonsyndromic deafness 49
Synonyms: autosomal recessive deafness 49, DFNB49
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with moderate to profound, stable hearing loss and has_material_basis_in mutation in the MARVELD2 gene on chromosome 5q13.
Ontology: Human Disease [DOID:0110506]   ( DOID:0110506 )

Relationships
is a type of: autosomal recessive nonsyndromic deafness