Hearing loss, autosomal recessive 107

Synonyms: Deafness, autosomal recessive 107

Available tests

6 tests are in the database for this condition.

Clinical tests (6 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

WBP2
14 tests
Also known as: DFNB107, GRAMD6, WBP-2, WBP2
Summary: WW domain binding protein 2

Imported from Human Phenotype Ontology (HPO)

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Ear malformation
- Hearing impairment
  Hearing impairment
  - MedGen UID: 235586
  - Concept ID: C1384666
  - Finding: Disease or Syndrome
  Ear malformation
  See: Feature record | Search on this feature

Reviews

Clinical resources

Molecular resources

Consumer resources

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