microphthalmia/coloboma 13
MONDO:0975809Mondo
Findings
No curated finding names microphthalmia/coloboma 13 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
- Congenital onset
HPO, annotations 2026-09-02
Features
18 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.
- AnophthalmiaHPOHP:0000528
- 3 of 3 reported patients
- BlindnessHPOHP:0000618
- 2 of 2 reported patients
- Chorioretinal atrophyHPOHP:0000533
- 1 of 1 reported patient
- ColobomaHPOHP:0000589
- 2 of 2 reported patients
- EsotropiaHPOHP:0000565
- 1 of 1 reported patient
- GlaucomaHPOHP:0000501
- 1 of 1 reported patient
- Global developmental delayHPOHP:0001263
- 1 of 1 reported patient
- High myopiaHPOHP:0011003
- 3 of 3 reported patients
- MicrocorneaHPOHP:0000482
- 1 of 1 reported patient
- MicrophthalmiaHPOHP:0000568
- 6 of 6 reported patients
- MyopiaHPOHP:0000545
- 1 of 1 reported patient
- Nuclear cataractHPOHP:0100018
- 1 of 1 reported patient
Show the remaining 6
- NystagmusHPOHP:0000639
- 4 of 4 reported patients
- Optic disc colobomaHPOHP:0000588
- 3 of 3 reported patients
- Retinal atrophyHPOHP:0001105
- 1 of 1 reported patient
- Retinal detachmentHPOHP:0000541
- 1 of 1 reported patient
- Retinal perforationHPOHP:0011958
- 1 of 1 reported patient
- StrabismusHPOHP:0000486
- 1 of 1 reported patient