U.S. flag

An official website of the United States government

GTR Home > Tests > Hearing Loss, Comprehensive Panel

Indication

This is a clinical test intended for Help: Diagnosis

Clinical summary

Help

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the ACTG1 gene. [from MONDO]

Clinical features

Help

Imported from Human Phenotype Ontology (HPO)

  • Bilateral sensorineural hearing impairment
  • Progressive sensorineural hearing impairment

Conditions tested

Target population

Help

Not provided

Clinical validity

Help

Not provided

Clinical utility

Help

Not provided

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.