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Concept information

disease > cardiovascular disease > Watson syndrome
disease > genetic disease > hereditary disease > Watson syndrome
disease > developmental disorder > mental retardation > Watson syndrome
disease > disability > mental retardation > Watson syndrome
disease > developmental disorder > growth retardation > Watson syndrome
... > disease > cardiovascular disease > heart disease > valvular heart disease > pulmonary valve stenosis > Watson syndrome
... > disease > skin appendages disease > skin disease > pigmentation disorder > café au lait spot > Watson syndrome

Preferred term

Watson syndrome  

Definition(s)

  • 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.Watson syndrome is allelic to NF1, the same gene associated with neurofibromatosis type 1. (Wikipedia)

Broader concept(s)

Synonym(s)

  • cafe au lait spots with pulmonic stenosis

In other languages

URI

http://data.loterre.fr/ark:/67375/VH8-RZR694NR-W

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