Details of Disease

General Information of Disease (ID: DISN52AL)

Disease Name Hearing loss, autosomal dominant 89
Disease Hierarchy
DISYC1G0: Autosomal dominant nonsyndromic hearing loss
DISN52AL: Hearing loss, autosomal dominant 89
Disease Identifiers
MONDO ID
MONDO_0859528
UMLS CUI
C5830357
OMIM ID
620284
MedGen ID
1840993

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
ATOH1 OTBZYG2R Limited Autosomal dominant [1]
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References

1 Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1. Clin Genet. 2020 Oct;98(4):353-364. doi: 10.1111/cge.13817. Epub 2020 Aug 24.