Details of Disease | DrugMAP

General Information of Disease (ID: DIS3YGUR)

Disease Name	Hearing loss, autosomal recessive 94
Synonyms	DFNB94; deafness, autosomal recessive 94
Disease Hierarchy	DIS8G9R9: Hearing loss, autosomal recessive DIS3YGUR: Hearing loss, autosomal recessive 94
Disease Identifiers	MONDO ID MONDO_0032749 UMLS CUI C5193096 OMIM ID 618434 MedGen ID 1679077

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
NARS2	OTL5X535	Limited	Autosomal recessive	[1]
------------------------------------------------------------------------------------

References

1	Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome. PLoS Genet. 2015 Mar 25;11(3):e1005097. doi: 10.1371/journal.pgen.1005097. eCollection 2015 Mar.