ORPHA:99642
Spondyloepimetaphyseal dysplasia, Handigodu type
- Body system
- Bone diseases
- Inheritance pattern
- Not documented in Orphadata
- Typical age of onset
- Adolescent, Adult, Childhood
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:99642 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Arthralgia of the hip
- Limited hip movement
- Hip osteoarthritis
- Gait disturbance
- Abnormality of the skeletal system
- Abnormality of the vertebral column