Details of Disease | DrugMAP

General Information of Disease (ID: DISE6HNY)

Disease Name	Hearing loss, autosomal dominant 77
Synonyms	DFNA77; deafness, autosomal dominant 77
Disease Hierarchy	DISYC1G0: Autosomal dominant nonsyndromic hearing loss DISE6HNY: Hearing loss, autosomal dominant 77
Disease Identifiers	MONDO ID MONDO_0030058 UMLS CUI C5394499 OMIM ID 618915 MedGen ID 1709284

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTP Molecule(s)

Gene Name	DTP ID	Evidence Level	Mode of Inheritance	REF
ABCC1	DTSYQGK	Moderate	Autosomal dominant	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
ABCC1	OTGUN89S	Moderate	Autosomal dominant	[1]
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References

1	Extrusion pump ABCC1 was first linked with nonsyndromic hearing loss in humans by stepwise genetic analysis. Genet Med. 2019 Dec;21(12):2744-2754. doi: 10.1038/s41436-019-0594-y. Epub 2019 Jul 5.