Hearing loss, autosomal dominant 37

Synonyms: Deafness, autosomal dominant 37

Summary

DFNA37 is an autosomal dominant form of early-onset postlingual progressive hearing impairment (Booth et al., 2019). [from OMIM]

Available tests

15 tests are in the database for this condition.

Clinical tests (15 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

COL11A1
196 tests
Also known as: CO11A1, COLL6, DFNA37, STL2, COL11A1
Summary: collagen type XI alpha 1 chain

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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