oculovertebral syndrome
MONDO:0979866Mondo
Findings
No curated finding names oculovertebral syndrome 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
- Congenital onset
HPO, annotations 2026-09-02
Features
27 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.
- AmblyopiaHPOHP:0000646
- 1 of 1 reported patient
- AstigmatismHPOHP:0000483
- 1 of 1 reported patient
- CataractHPOHP:0000518
- 1 of 1 reported patient
- Cortical cataractHPOHP:0100019
- 2 of 2 reported patients
- HemorrhoidsHPOHP:0032551
- 1 of 1 reported patient
- MicrocorneaHPOHP:0000482
- 2 of 2 reported patients
- MicrognathiaHPOHP:0000347
- 1 of 1 reported patient
- MicrophthalmiaHPOHP:0000568
- 1 of 1 reported patient
- Mitral valve prolapseHPOHP:0001634
- 1 of 1 reported patient
- MyopiaHPOHP:0000545
- 3 of 3 reported patients
- NystagmusHPOHP:0000639
- 2 of 2 reported patients
- Posterior subcapsular cataractHPOHP:0007787
- 1 of 1 reported patient
Show the remaining 15
- Retinal perforationHPOHP:0011958
- 1 of 1 reported patient
- ScoliosisHPOHP:0002650
- 4 of 4 reported patients
- Sensorineural hearing impairmentHPOHP:0000407
- 1 of 1 reported patient
- Spina bifidaHPOHP:0002414
- 1 of 1 reported patient
- Spina bifida occultaHPOHP:0003298
- 2 of 2 reported patients
- StrabismusHPOHP:0000486
- 1 of 1 reported patient
Where it sits
- A kind of