Weill-Marchesani Syndrome
MeSH code information
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Name
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ConceptScope 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.
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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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Qualifiersdiagnosis, 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