Details of Disease

General Information of Disease (ID: DISGBZRR)

Disease Name Autosomal dominant nonsyndromic hearing loss 11
Synonyms
autosomal dominant nonsyndromic deafness 11; autosomal dominant nonsyndromic deafness type 11; autosomal dominant nonsyndromic deafness caused by mutation in MYO7A; deafness, autosomal dominant 11; MYO7A autosomal dominant nonsyndromic deafness; autosomal dominant deafness 11; deafness, autosomal dominant type 11; DFNA11
Definition Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYO7A gene.
Disease Hierarchy
DISYC1G0: Autosomal dominant nonsyndromic hearing loss
DISGBZRR: Autosomal dominant nonsyndromic hearing loss 11
Disease Identifiers
MONDO ID
MONDO_0011032
MESH ID
C563353
UMLS CUI
C1832475
OMIM ID
601317
MedGen ID
331297

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
MYO7A OTBZSPEL Strong Autosomal dominant [1]
------------------------------------------------------------------------------------

References

1 Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene. Nat Genet. 1997 Nov;17(3):268-9. doi: 10.1038/ng1197-268.