Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders

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.

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2.

OMIM.ORG article

Omim 616705 [^]
Update: April 29, 2019