omodysplasia
MONDO:0017136Mondo
Findings
No curated finding names omodysplasia yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Omodysplasia is a rare skeletal dysplasia characterized by severe limb shortening and facial dysmorphism. Two types of omodysplasia have been described: an autosomal recessive or generalized form (also referred to as micromelic dysplasia with dislocation of radius) marked by severe micromelic dwarfism with predominantly rhizomelic shortening of both the upper and lower limbs, and an autosomal dominant form in which stature is normal and shortening is limited to the upper limbs.
Definition from the Mondo Disease Ontology (MONDO:0017136), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
- Narrower terms (2)