DISEASES

Disease-gene associations mined from literature

Human genes for autosomal recessive nonsyndromic deafness 101

Autosomal recessive nonsyndromic deafness 101 [DOID:0110462]

An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the GRXCR2 gene on chromosome 5q32.

Synonyms:  autosomal recessive nonsyndromic deafness 101,  DOID:0110462,  DFNB101,  autosomal recessive deafness 101