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autosomal recessive nonsyndromic deafness 44

Disease Summary
Associated Targets (1)
Tchem

1


Mondo Description Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the ADCY1 gene.
Uniprot Description A form of non-syndromic deafness characterized by prelingual profound hearing loss affecting all frequencies.
Mondo Term and Equivalent IDs
MONDO:0012421:  autosomal recessive nonsyndromic deafness 44
MESH:C565716: 
UMLS:C1857809: