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autosomal recessive nonsyndromic deafness 39

Disease Summary
Associated Targets (1)
Tchem

1


Mondo Description An autosomal recessive disorder caused by mutations in the HGF gene, encoding hepatocyte growth factor receptor. It is characterized by profound deafness.
Uniprot Description A form of profound prelingual 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.
Mondo Term and Equivalent IDs
MONDO:0012003:  autosomal recessive nonsyndromic deafness 39
MESH:C564265: 
NCIT:C129874: 
UMLS:C1842342: