Weill-Marchesani Syndrome

MeSH code information
  • Name
  • Concept
    Scope note:Rare congenital disorder of connective tissue characterized by brachydactyly, joint stiffness, childhood onset of ocular abnormalities (e.g., microspherophakia, ECTOPIA LENTIS; GLAUCOMA), and proportionate short stature. Cardiovascular anomalies are occasionally seen.
  • Tree numbers
    • C05.116.099.343.957
    • C11.270.921
    • C16.131.077.941
    • C16.320.290.842
    • C17.300.899
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