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
  • Qualifiers
    diagnosis, parasitology, immunology, microbiology, diagnostic imaging, physiopathology, rehabilitation, enzymology, etiology, mortality, epidemiology, blood, cerebrospinal fluid, chemically induced, diet therapy, drug therapy, therapy, psychology, urine, virology, veterinary, history, classification, economics, embryology, genetics, nursing, radiotherapy, ethnology, prevention & control, pathology, metabolism, complications, surgery
Filters
Contact
Chat with gentaur.com employee