ORPHA:321
Multiple osteochondromas
Also called Bessel-Hagen disease, Multiple cartilaginous exostoses
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Childhood
- Estimated prevalence
- >1 / 1000 (Specific population)
- Rarity class
- >1 / 1000
ORPHA:321 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Limitation of joint mobility
- Abnormal cartilage morphology
- Abnormality of the knee
- Abnormality of femur morphology
- Abnormal bone structure
- Deformed forearm bones