Hearing loss, autosomal recessive 113

Synonyms: Deafness, autosomal recessive 113

Summary

DFNB113 is characterized by postlingual progressive hearing impairment (Booth et al., 2018). [from OMIM]

Available tests

5 tests are in the database for this condition.

Clinical tests (5 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

CEACAM16
35 tests
Also known as: CEAL2, DFNA4B, DFNB113, CEACAM16
Summary: CEA cell adhesion molecule 16, tectorial membrane component

Imported from Human Phenotype Ontology (HPO)

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Ear malformation
- Abnormal vestibular function
  Abnormal vestibular function
  - MedGen UID: 334848
  - Concept ID: C1843865
  - Finding: Finding
  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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