Autosomal dominant nonsyndromic hearing loss 67

Synonyms: Deafness, autosomal dominant 67

Summary

DFNA67 is a form of nonsyndromic sensorineural hearing loss. Onset ranges from the first to the fourth year of life. Hearing loss initially affects high frequencies, with variable progression. There are no vestibular symptoms (Xing et al., 2015; Thoenes et al., 2015). [from OMIM]

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.

OSBPL2
25 tests
Also known as: DFNA67, DNFA67, ORP-2, ORP2, OSBPL2
Summary: oxysterol binding protein like 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
- Tinnitus
  Tinnitus
  - MedGen UID: 52760
  - Concept ID: C0040264
  - Finding: Disease or Syndrome
  Ear malformation
  See: Feature record | Search on this feature

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Molecular resources

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