Autosomal recessive nonsyndromic hearing loss 24

Synonyms: DFNB24 Nonsyndromic Hearing Loss and Deafness; Deafness, autosomal recessive 24

Summary

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

Available tests

20 tests are in the database for this condition.

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Clinical tests (20 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

RDX
36 tests
Also known as: DFNB24, RDX
Summary: radixin

Imported from Human Phenotype Ontology (HPO)

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Ear malformation
- Profound sensorineural hearing impairment
  Profound sensorineural hearing impairment
  - MedGen UID: 868926
  - Concept ID: C4023338
  - Finding: Disease or Syndrome
  Ear malformation
  See: Feature record | Search on this feature

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