Hereditary deafness 97

Hereditary deafness 97 is an autosomal recessive disorder caused by mutations of the MET gene.

Systematic

Hereditary deafness
	Alport Syndrome
	Autosomal recesive deafness 12
	Autosomal recessive deafness 23
	Autosomal recessive deafness 4 with enlarged vestibular aqueduct
	Enlarged vestibular aqueduct
	Hereditary deafness 97
		MET
	IVIC syndrome
	MYH9 related disorders
	Stapes ankylosis with broad thumbs and toes
	Usher syndrome
	X-linked non-syndromic sensorineural deafness type DFN

References:

1.	Mujtaba G et al. (2015) A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss.

2.	OMIM.ORG article Omim 616705

Update: Aug. 14, 2020

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