Stargardt disease 3
MONDO:0010819Mondo
Findings
No curated finding names Stargardt disease 3 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
5 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.
- Macular atrophyHPOHP:0007401
- Macular dystrophyHPOHP:0007754
- Macular flecksHPOHP:0011507
- Reduced visual acuityHPOHP:0007663
- Visual impairmentHPOHP:0000505
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.
- ELOVL4HGNC:14415
- Definitive · G2P · Autosomal dominant · 2017
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2020
Where it sits
Other names
1 name
Resolves to: Stargardt disease 3
- Also called
- Stargardt disease type 3