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bn:01758275n
Noun Concept
SYL
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
EN
disease
EN
rare disease
EN
pulmonary valve stenosis
GENETIC ASSOCIATION
EN
neurofibromin 1
HEALTH SPECIALTY
EN
medical genetics

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