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autosomal recessive nonsyndromic deafness 8

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description An autosomal recessive nonsyndromic deafness that has material basis in mutation in the TMPRSS3 gene on chromosome 21q22.
Uniprot Description A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information.
Disease Ontology Description An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the TMPRSS3 gene on chromosome 21q22.
Mondo Term and Equivalent IDs
MONDO:0010987:  autosomal recessive nonsyndromic deafness 8
UMLS:C1832827: