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autosomal recessive nonsyndromic deafness 26

Disease Summary
Associated Targets (1)
Tchem

1


Mondo Description An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 4q31.
Uniprot Description A form of non-syndromic sensorineural deafness characterized by prelingual, severe to profound 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.
Mondo Term and Equivalent IDs
MONDO:0011553:  autosomal recessive nonsyndromic deafness 26
MESH:C565329: 
UMLS:C1854275: