Autosomal dominant nonsyndromic hearing loss 68

Synonyms: Deafness, autosomal dominant 68

Summary

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the HOMER2 gene. [from MONDO]

Available tests

10 tests are in the database for this condition.

Clinical tests (10 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

HOMER2
23 tests
Also known as: ACPD, CPD, DFNA68, HOMER-2, VESL-2, HOMER2
Summary: homer scaffold protein 2

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

Reviews

Clinical resources

Molecular resources

Consumer resources

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