Details of Disease | DrugMAP

General Information of Disease (ID: DISTAS5Z)

Disease Name	Hearing loss, autosomal dominant 72
Synonyms	deafness, autosomal dominant 72; autosomal dominant nonsyndromic deafness 72; DFNA72
Disease Hierarchy	DISYC1G0: Autosomal dominant nonsyndromic hearing loss DISTAS5Z: Hearing loss, autosomal dominant 72
Disease Identifiers	MONDO ID MONDO_0033259 UMLS CUI C4539886 OMIM ID 617606 MedGen ID 1614203

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
SLC44A4	TT0NYDG	Limited	Genetic Variation	[1]
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This Disease Is Related to 1 DTP Molecule(s)

Gene Name	DTP ID	Evidence Level	Mode of Inheritance	REF
SLC44A4	DT8KXR9	Limited	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
SLC44A4	OT1HIORM	Limited	Autosomal dominant	[1]
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References

1	SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss. Hum Mol Genet. 2017 Jan 15;26(2):383-394.