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bn:01758275n
Noun Concept
IT
No term available
EN
Watson syndrome is an autosomal dominant condition characterized by Lisch nodules of the ocular iris, axillary/inguinal freckling, pulmonary valvular stenosis, relative macrocephaly, short stature, and neurofibromas. Wikipedia
Relations
Sources
IS A
malattia
malattia rara
stenosi della valvola polmonare
GENETIC ASSOCIATION
neurofibromina 1
HEALTH SPECIALTY
genetica clinica

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