Details of Disease | DrugMAP

General Information of Disease (ID: DISPPMAF)

Disease Name	Hearing loss, autosomal dominant 37
Synonyms	DEAFNESS, AUTOSOMAL DOMINANT 37; deafness, autosomal dominant 37; DFNA37
Disease Hierarchy	DISYC1G0: Autosomal dominant nonsyndromic hearing loss DISPPMAF: Hearing loss, autosomal dominant 37
Disease Identifiers	MONDO ID MONDO_0032802 UMLS CUI C4760307 OMIM ID 618533 MedGen ID 1676950

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
COL11A1	OTB0DRMS	Strong	Autosomal dominant	[1]
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References

1	Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37. Genet Med. 2019 Apr;21(4):948-954. doi: 10.1038/s41436-018-0285-0. Epub 2018 Sep 24.