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autosomal recessive nonsyndromic deafness 97

Disease Summary
Associated Targets (1)
Tclin

1


Mondo Description Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MET gene.
Uniprot Description A form of non-syndromic sensorineural hearing loss with prelingual onset. 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 MET gene on chromosome 7q31.
Mondo Term and Equivalent IDs
MONDO:0014739:  autosomal recessive nonsyndromic deafness 97
UMLS:C4084709: