Details of Disease | DrugMAP

General Information of Disease (ID: DIS7CFPD)

Disease Name	Hearing loss, autosomal recessive 115
Synonyms	DFNB115; deafness, autosomal recessive 115
Disease Hierarchy	DIS8G9R9: Hearing loss, autosomal recessive DIS7CFPD: Hearing loss, autosomal recessive 115
Disease Identifiers	MONDO ID MONDO_0032762 UMLS CUI C5193108 OMIM ID 618457 MedGen ID 1681630

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTP Molecule(s)

Gene Name	DTP ID	Evidence Level	Mode of Inheritance	REF
SPNS2	DT3Q1UO	Moderate	Autosomal recessive	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
SPNS2	OTPODAPU	Moderate	Autosomal recessive	[1]
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References

1	Mouse screen reveals multiple new genes underlying mouse and human hearing loss. PLoS Biol. 2019 Apr 11;17(4):e3000194. doi: 10.1371/journal.pbio.3000194. eCollection 2019 Apr.