Meier-Gorlin syndrome 10
MONDO:0981050Mondo
Findings
No curated finding names Meier-Gorlin syndrome 10 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 · Fetal onset
HPO, annotations 2026-09-02
Features
86 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.
- Acetabular dysplasiaHPOHP:0008807
- 1 of 1 reported patient
- Atrial septal defectHPOHP:0001631
- 1 of 1 reported patient
- Birth length less than 3rd percentileHPOHP:0003561
- 2 of 2 reported patients
- BrachydactylyHPOHP:0001156
- 1 of 1 reported patient
- Clinodactyly of the 5th fingerHPOHP:0004209
- 1 of 1 reported patient
- Clitoral hypertrophyHPOHP:0008665
- 1 of 1 reported patient
- ClubbingHPOHP:0001217
- 1 of 1 reported patient
- Congenital knee dislocationHPOHP:0005191
- 1 of 1 reported patient
- Convex nasal ridgeHPOHP:0000444
- 1 of 1 reported patient
- Craniofacial dystoniaHPOHP:0012179
- 1 of 1 reported patient
- CryptorchidismHPOHP:0000028
- 1 of 1 reported patient
- Delayed ability to walkHPOHP:0031936
- 1 of 1 reported patient
Show the remaining 74
- Delayed skeletal maturationHPOHP:0002750
- 2 of 2 reported patients
- Depressed nasal bridgeHPOHP:0005280
- 1 of 1 reported patient
- Dislocated radial headHPOHP:0003083
- 1 of 1 reported patient
- Downslanted palpebral fissuresHPOHP:0000494
- 1 of 1 reported patient
- DysphagiaHPOHP:0002015
- 1 of 1 reported patient
- Failure to thriveHPOHP:0001508
- 2 of 2 reported patients
Where it sits
- A kind of