Autosomal dominant nonsyndromic hearing loss 12

Synonyms: DEAFNESS, AUTOSOMAL DOMINANT 8; DFNA 8/12 Nonsyndromic Hearing Loss and Deafness; Deafness, autosomal dominant 12

Summary

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

Available tests

24 tests are in the database for this condition.

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Clinical tests (24 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

TECTA
49 tests
Also known as: DFNA12, DFNA8, DFNB21, TECTA
Summary: tectorin alpha

Imported from Human Phenotype Ontology (HPO)

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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

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