Stargardt disease 5
MONDO:0980722Mondo
Findings
No curated finding names Stargardt disease 5 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Middle age onset
HPO, annotations 2026-09-02
Features
8 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.
- Abnormal electroretinogramHPOHP:0000512
- 1 of 1 reported patient
- Central thinning of the outer nuclear layer of the retinaHPOHP:6000367
- 1 of 1 reported patient
- HypertensionHPOHP:0000822
- 1 of 1 reported patient
- Mildly reduced visual acuityHPOHP:0032037
- 1 of 1 reported patient
- Ocular hypertensionHPOHP:0007906
- 1 of 1 reported patient
- Retinal flecksHPOHP:0012045
- 1 of 1 reported patient
- Retinal pigment epithelial atrophyHPOHP:0007722
- 1 of 1 reported patient
- Subretinal depositsHPOHP:0031528
- 1 of 1 reported patient
Where it sits
- A kind of