Details of Disease | DrugMAP

General Information of Disease (ID: DIS9NTR8)

Disease Name	Autosomal recessive nonsyndromic hearing loss 97
Synonyms	autosomal recessive nonsyndromic deafness 97; MET autosomal recessive nonsyndromic deafness; DFNB97; deafness, autosomal recessive type 97; autosomal recessive nonsyndromic deafness caused by mutation in MET; autosomal recessive deafness 97; deafness, autosomal recessive 97; autosomal recessive nonsyndromic deafness type 97
Definition	Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MET gene.
Disease Hierarchy	DIS8G9R9: Hearing loss, autosomal recessive DIS9NTR8: Autosomal recessive nonsyndromic hearing loss 97
Disease Identifiers	MONDO ID MONDO_0014739 UMLS CUI C4084709 OMIM ID 616705 MedGen ID 899875

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 2 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
MET	TTNDSF4	Strong	Autosomal recessive	[1]
MET	TTNDSF4	Strong	Genetic Variation	[2]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
MET	OT7K55MU	Strong	Autosomal recessive	[1]
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References

1	A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss. J Med Genet. 2015 Aug;52(8):548-52. doi: 10.1136/jmedgenet-2015-103023. Epub 2015 May 4.
2	Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness.Hum Hered. 2019;84(3):109-116. doi: 10.1159/000503450. Epub 2019 Dec 4.