Autosomal dominant nonsyndromic hearing loss 27

Synonyms: Deafness, autosomal dominant 27

Summary

DFNA27 is characterized by postlingual progressive moderate to profound sensorineural hearing loss (Peters et al., 2008). [from OMIM]

Available tests

5 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (5 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

REST
Also known as: DFNA27, GINGF5, HGF5, NRSF, WT6, XBR, REST
Summary: RE1 silencing transcription factor

Imported from Human Phenotype Ontology (HPO)

Show all Hide all

Ear malformation
- Sensorineural hearing loss disorder
  Sensorineural hearing loss disorder
  - MedGen UID: 9164
  - Concept ID: C0018784
  - Finding: Disease or Syndrome
  Ear malformation
  See: Feature record | Search on this feature

Reviews

Clinical resources

Molecular resources

Consumer resources

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.