cataract 20 multiple types
MONDO:0007284Mondo
Findings
No curated finding names cataract 20 multiple types yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any cataract (disease) in which the cause of the disease is a mutation in the CRYGS gene.
Definition from the Mondo Disease Ontology (MONDO:0007284), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Juvenile onset
HPO, annotations 2026-09-02
Features
4 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Cortical cataractHPOHP:0100019
- 14 of 14 reported patients
- Lamellar cataractHPOHP:0007971
- 4 of 4 reported patients
- Nuclear cataractHPOHP:0100018
- 7 of 7 reported patients · Congenital onset
- Sutural cataractHPOHP:0010695
- 4 of 4 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- CRYGSHGNC:2417
- Definitive · G2P · Autosomal dominant · 2017
- Strong · Ambry Genetics · Autosomal dominant · 2023
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2021
Where it sits
- A kind of
Other names
3 names
Resolves to: cataract 20 multiple types
- Also called
- cataract (disease) caused by mutation in CRYGSCRYGS cataract (disease)CTRCT20