Details of Disease | DrugMAP

General Information of Disease (ID: DIS78B8D)

Disease Name	Hearing loss, autosomal dominant 82
Synonyms	deafness, autosomal dominant 82; DFNA82
Disease Hierarchy	DISYC1G0: Autosomal dominant nonsyndromic hearing loss DIS78B8D: Hearing loss, autosomal dominant 82
Disease Identifiers	MONDO ID MONDO_0030719 UMLS CUI C5676948 OMIM ID 619804 MedGen ID 1803416

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
ATP2B2	OT1NPZ9T	Strong	Autosomal dominant	[1]
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References

1	Modification of human hearing loss by plasma-membrane calcium pump PMCA2. N Engl J Med. 2005 Apr 14;352(15):1557-64. doi: 10.1056/NEJMoa043899.