Cataract 45

Summary

Any early-onset non-syndromic cataract in which the cause of the disease is a mutation in the SIPA1L3 gene. [from MONDO]

Available tests

4 tests are in the database for this condition.

Clinical tests (4 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

SIPA1L3
14 tests
Also known as: CTRCT45, SPAL3, SPAR3, SIPA1L3
Summary: signal induced proliferation associated 1 like 3

Imported from Human Phenotype Ontology (HPO)

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Abnormality of the eye
- Developmental cataract
  Developmental cataract
  - MedGen UID: 3202
  - Concept ID: C0009691
  - Finding: Congenital Abnormality
  Abnormality of the eye
  See: Feature record | Search on this feature

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