Autosomal dominant nonsyndromic hearing loss 56

Synonyms: Deafness, autosomal dominant 56

Summary

Autosomal dominant deafness-56 is a form of nonsyndromic sensorineural hearing loss. Hearing impairment shows postlingual onset and is progressive (summary by Zhao et al., 2013). [from OMIM]

Available tests

15 tests are in the database for this condition.

Clinical tests (15 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

TNC
27 tests
Also known as: 150-225, DFNA56, GMEM, GP, HXB, JI, TN, TN-C, TNC
Summary: tenascin C

Imported from Human Phenotype Ontology (HPO)

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Ear malformation
- Abnormal vestibular function
  Abnormal vestibular function
  - MedGen UID: 334848
  - Concept ID: C1843865
  - Finding: Finding
  Ear malformation
  See: Feature record | Search on this feature
- 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

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