cataract 30
MONDO:0007286Mondo
Findings
No curated finding names cataract 30 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A cataract that has material basis in heterozygous mutation in the VIM gene on chromosome 10p13.
Definition from the Mondo Disease Ontology (MONDO:0007286), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Congenital onset
HPO, annotations 2026-09-02
Features
3 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.
- Diffuse nuclear cataractHPOHP:0007657
- 1 of 1 reported patient
- Posterior polar cataractHPOHP:0001115
- 2 of 2 reported patients
- Pulverulent cataractHPOHP:0010693
- 1 of 1 reported patient
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.
- VIMHGNC:12692
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2021
- Strong · PanelApp Australia · Autosomal dominant · 2025
Where it sits
- A kind of
Other names
2 names
Resolves to: cataract 30
- Also called
- cataract type 30CTRCT30