Genochondromatosis Type 2 C4511481
A rare genetic disorder causing benign cartilaginous tumors on bones, potentially leading to bone deformities. Surgical removal is typically the primary treatment approach when symptoms become problematic.
Key facts at a glance
- ICD-10
- Q79.9
- ICD-11
- LA00.0
- Body system
- musculoskeletal
- Severity
- moderate
- Chronic
- true
Frequently asked questions
Common questions about this topic.
What is Genochondromatosis Type 2 C4511481?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy