autosomal recessive nonsyndromic deafness 49 (DOID:0110506)
Alliance: disease page
Synonyms: autosomal recessive deafness 49; DFNB49
Alt IDs: OMIM:610153, ICD10CM:H90.3
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.