Hearing loss, autosomal dominant 75

Synonyms: Deafness, autosomal dominant 75

Summary

DFNA75 is characterized by adult onset of moderate to severe, mid to high frequency hearing loss, progressing to involvement of all frequencies (Xia et al., 2019). [from OMIM]

Available tests

8 tests are in the database for this condition.

Clinical tests (8 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

TRRAP
21 tests
Also known as: DEDDFA, DFNA75, PAF350/400, PAF400, STAF40, TR-AP, Tra1, TRRAP
Summary: transformation/transcription domain associated protein

Imported from Human Phenotype Ontology (HPO)

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Ear malformation
- Abnormal cochlea morphology
  Abnormal cochlea morphology
  - MedGen UID: 871363
  - Concept ID: C4025858
  - Finding: Anatomical Abnormality
  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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