Autosomal recessive nonsyndromic hearing loss 88

Synonyms: Deafness, autosomal recessive 88

Summary

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the ELMOD3 gene. [from MONDO]

Available tests

8 tests are in the database for this condition.

Clinical tests (8 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

ELMOD3
23 tests
Also known as: DFNA81, DFNB88, LST3, RBED1, RBM29, ELMOD3
Summary: ELMO domain containing 3

Imported from Human Phenotype Ontology (HPO)

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Ear malformation
- Mixed hearing impairment
  Mixed hearing impairment
  - MedGen UID: 102336
  - Concept ID: C0155552
  - Finding: Disease or Syndrome
  Ear malformation
  See: Feature record | Search on this feature

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Clinical resources

Molecular resources

Consumer resources

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