Details of Disease | DrugMAP

General Information of Disease (ID: DISIP6W8)

Disease Name	Hearing loss, autosomal dominant 87
Disease Hierarchy	DISYC1G0: Autosomal dominant nonsyndromic hearing loss DISIP6W8: Hearing loss, autosomal dominant 87
Disease Identifiers	MONDO ID MONDO_0859525 UMLS CUI C5830342 OMIM ID 620281 MedGen ID 1840978

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
PI4KB	TTNPL3B	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
PI4KB	OTI9UQSU	Limited	Autosomal dominant	[1]
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References

1	Identification and functional characterization of two novel mutations in KCNJ10 and PI4KB in SeSAME syndrome without electrolyte imbalance. Hum Genomics. 2019 Oct 22;13(1):53. doi: 10.1186/s40246-019-0236-0.