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bn:01758275n
Noun Concept
NL
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
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Sources
IS A
ziekte
zeldzame ziekte
pulmonalisstenose
GENETIC ASSOCIATION
NF1
HEALTH SPECIALTY
medische genetica

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