Cataract 38

Synonyms: Cataract 38, autosomal recessive; Cataract, autosomal recessive congenital 5

Summary

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

Available tests

42 tests are in the database for this condition.

Clinical tests (41 available)

Molecular Genetics Tests

Research tests

See all research tests for this condition (1)

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

AGK
114 tests
Also known as: CATC5, CTRCT38, MTDPS10, MULK, AGK
Summary: acylglycerol kinase

Imported from Human Phenotype Ontology (HPO)

Show all Hide all

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

Reviews

Clinical resources

Molecular resources

Consumer resources

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.