optic atrophy 8
MONDO:0024569Mondo
Findings
No curated finding names optic atrophy 8 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
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.
- Central scotomaHPOHP:0000603
- 5 of 5 reported patients
- Abnormal auditory evoked potentialsHPOHP:0006958
- 3 of 5 reported patients
- Mitral valve prolapseHPOHP:0001634
- 3 of 5 reported patients
- Abnormality of pattern visual evoked potentialsHPOHP:0030455
- Optic atrophyHPOHP:0000648
- Prolonged somatosensory evoked potentialsHPOHP:0007104
- Sensorineural hearing impairmentHPOHP:0000407
- Visual impairmentHPOHP:0000505
Where it sits
Other names
1 name
Resolves to: optic atrophy 8
- Also called
- OPA8