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bn:03438050n
Noun Concept
NL
Noonan Syndrome with Multiple Lentigines  leopard syndroom
EN
Noonan syndrome with multiple lentigines which is part of a group called Ras/MAPK pathway syndromes, is a rare autosomal dominant, multisystem disease caused by a mutation in the protein tyrosine phosphatase, non-receptor type 11 gene. Wikipedia
Relations
Sources
IS A
zeldzame ziekte
EN
RASopathy
GENETIC ASSOCIATION
BRAF
RAF1
PTPN11
HEALTH SPECIALTY
cardiologie
dermatologie
reumatologie
Wikidata
NL
Noonan Syndrome with Multiple Lentigines
Wikipedia Translations
NL
leopard syndroom

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