Singleton Merten Syndrome 2 C4225380
A rare genetic disorder affecting bones, teeth, and muscles, often causing weakness and skeletal abnormalities. It may involve heart and metabolic issues as well. Care is supportive and focuses on managing symptoms and preventing complications.
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 pain or stiffness
(musculoskeletal)Significant symptoms that substantially affect daily functioning.
Frequency: Common at all stages
Medication Comparisons
Compare medications used to treat Singleton Merten Syndrome 2 C4225380. 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