Hearing loss, autosomal dominant 73

Synonyms: Deafness, autosomal dominant 73

Available tests

7 tests are in the database for this condition.

Clinical tests (7 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

PTPRQ
26 tests
Also known as: DFNA73, DFNB84, DFNB84A, PTPGMC1, R-PTP-Q, PTPRQ
Summary: protein tyrosine phosphatase receptor type Q

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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Clinical resources

Molecular resources

Consumer resources

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