ORPHA:93349
X-linked spondyloepimetaphyseal dysplasia
- Body system
- Bone diseases
- Inheritance pattern
- X-linked recessive
- Typical age of onset
- Not documented in Orphadata
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:93349 is classified under "Bone diseases" in the Orphanet nomenclature.