Retinitis pigmentosa 55

Summary

Any retinitis pigmentosa in which the cause of the disease is a mutation in the ARL6 gene. [from MONDO]

Available tests

39 tests are in the database for this condition.

Clinical tests (39 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

ARL6
135 tests
Also known as: BBS3, RP55, ARL6
Summary: ARF like GTPase 6

Imported from Human Phenotype Ontology (HPO)

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Abnormality of the eye
- Rod-cone dystrophy
  Rod-cone dystrophy
  - MedGen UID: 1632921
  - Concept ID: C4551714
  - Finding: Disease or Syndrome
  Abnormality of the eye
  See: Feature record | Search on this feature

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Clinical resources

Molecular resources

Consumer resources

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