short stature, Brussels type
MONDO:0011046Mondo
Findings
No curated finding names short stature, Brussels type yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
This syndrome is characterized by short stature presenting in the neonatal period associated with osteochondrodysplastic lesions and facial dysmorphism.
Definition from the Mondo Disease Ontology (MONDO:0011046), read 2026-09-29. CC BY 4.0.
Features
10 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 facial shapeHPOHP:0001999
- Very frequent (80% to 99% of cases)
- Growth delayHPOHP:0001510
- Very frequent (80% to 99% of cases)
- Short statureHPOHP:0004322
- Very frequent (80% to 99% of cases)
- Calcification of cartilageHPOHP:0100593
- Frequent (30% to 79% of cases)
- Delayed epiphyseal ossificationHPOHP:0002663
- Frequent (30% to 79% of cases)
- Horseshoe kidneyHPOHP:0000085
- Frequent (30% to 79% of cases)
- MacrocephalyHPOHP:0000256
- Frequent (30% to 79% of cases)
- MicroretrognathiaHPOHP:0000308
- Frequent (30% to 79% of cases)
- Narrow chestHPOHP:0000774
- Frequent (30% to 79% of cases)
- Triangular faceHPOHP:0000325
- Frequent (30% to 79% of cases)
Where it sits
Other names
1 name
Resolves to: short stature, Brussels type
- Also called
- Mievis-Verellen-Dumoulin syndrome