Chondrodysplasia With Joint Dislocations Gpapp Type C3279757
A rare genetic skeletal condition causing abnormal bone development and recurrent joint dislocations. Requires orthopedic management and multidisciplinary care to address mobility and joint problems.
Key facts at a glance
- ICD-10
- Q79.9
- ICD-11
- LA00.0
- Body system
- musculoskeletal
- Severity
- severe
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Joint dislocations
(musculoskeletal)Joint pain or stiffness
(musculoskeletal)Significant symptoms that substantially affect daily functioning.
Frequency: Common at all stages
Brachydactyly
(musculoskeletal)Short stature
(musculoskeletal)Cleft palate
(musculoskeletal)Medication Comparisons
Compare medications used to treat Chondrodysplasia With Joint Dislocations Gpapp Type C3279757. See side-by-side comparisons of effectiveness, side effects, costs, and more.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy