keratitis fugax hereditaria
MONDO:0007849Mondo
Findings
No curated finding names keratitis fugax hereditaria yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Juvenile onset · Young adult onset
HPO, annotations 2026-09-02
Features
6 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.
- KeratitisHPOHP:0000491
- 34 of 34 reported patients
- Opacification of the corneal stromaHPOHP:0007759
- 18 of 34 reported patients
- Epiretinal membraneHPOHP:0100014
- 2 of 34 reported patients
- Blurred visionHPOHP:0000622
- Conjunctival hyperemiaHPOHP:0030953
- PhotophobiaHPOHP:0000613
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.
- NLRP3HGNC:16400
- Limited · Ambry Genetics · Autosomal dominant · 2018
Where it sits
- A kind of
Other names
2 names
Resolves to: keratitis fugax hereditaria
- Also called
- keratoendotheliitis fugax hereditariakeratoendothelitis fugax hereditaria