ORPHA:253
Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
Also called SED and SEMD
- Body system
- Bone diseases
- Inheritance pattern
- Not documented in Orphadata
- Typical age of onset
- All ages
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:253 is classified under "Bone diseases" in the Orphanet nomenclature.