Weill Marchesani Syndrome 3 C3553785
A rare genetic connective tissue disorder causing short stature, short fingers, joint stiffness, and eye problems including small lenses and glaucoma. Inherited in an autosomal recessive pattern. Treatment focuses on managing symptoms like glaucoma and lens complications.
Key facts at a glance
- ICD-10
- Q89.9
- ICD-11
- LA00.0
- Body system
- congenital
- Severity
- moderate
- Chronic
- true
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 27, 2026. · Read our editorial policy