Details of Disease | DrugMAP

General Information of Disease (ID: DISTYHRQ)

Disease Name	Hearing loss, autosomal dominant 71
Synonyms	autosomal dominant nonsyndromic deafness 71; deafness, autosomal dominant 71; DFNA71
Disease Hierarchy	DISYC1G0: Autosomal dominant nonsyndromic hearing loss DISTYHRQ: Hearing loss, autosomal dominant 71
Disease Identifiers	MONDO ID MONDO_0033258 UMLS CUI C4539881 OMIM ID 617605 MedGen ID 1621646

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
DMXL2	OTB4JWN3	Limited	Autosomal dominant	[1]
------------------------------------------------------------------------------------

References

1	The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resources. Genet Med. 2022 Aug;24(8):1732-1742. doi: 10.1016/j.gim.2022.04.017. Epub 2022 May 4.