Autosomal recessive nonsyndromic hearing loss 22

Synonyms: DFNB22 Nonsyndromic Hearing Loss and Deafness; Deafness, autosomal recessive 22

Summary

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the OTOA gene. [from MONDO]

Available tests

18 tests are in the database for this condition.

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Clinical tests (18 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

OTOA
38 tests
Also known as: CT108, DFNB22, OTOA
Summary: otoancorin

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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