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GTR Home > Tests > MYO7A

Indication

This is a clinical test intended for Help: Screening

Clinical summary

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Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MYO7A gene. [from MONDO]

Clinical features

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Imported from Human Phenotype Ontology (HPO)

  • Sensorineural hearing impairment
  • Vertigo
  • Abnormal vestibular function

Conditions tested

Target population

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Not provided

Clinical validity

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Not provided

Clinical utility

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Not provided

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