Details of Disease

General Information of Disease (ID: DISTPVR5)

Disease Name Hearing loss, autosomal dominant 88
Disease Hierarchy
DISYC1G0: Autosomal dominant nonsyndromic hearing loss
DISTPVR5: Hearing loss, autosomal dominant 88
Disease Identifiers
MONDO ID
MONDO_0859527
UMLS CUI
C5830355
OMIM ID
620283
MedGen ID
1840991

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
EPHA10 OT1XJGFG Limited Autosomal dominant [1]
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References

1 Classification of Genes: Standardized Clinical Validity Assessment of Gene-Disease Associations Aids Diagnostic Exome Analysis and Reclassifications. Hum Mutat. 2017 May;38(5):600-608. doi: 10.1002/humu.23183. Epub 2017 Feb 13.