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bn:03438050n
Noun Concept
Categories: Genodermatoses, Neuro-cardio-facial-cutaneous syndromes, RASopathies, Melanocytic nevi and neoplasms, Syndromes affecting hearing
EN
LEOPARD syndrome  Noonan Syndrome with Multiple Lentigines  Generalized lentiginosis  Multiple lentigines syndrome  Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome
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
Definitions
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Sources
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
A rare autosomal dominant multisystem disease, associated with high numbers of surface skin lesions Wikipedia Disambiguation
Rare autosomal dominant,[3] multisystem disease caused by a mutation in the protein tyrosine phosphatase, non-receptor type 11 gene Wikidata
IS A
rare disease
RASopathy
GENETIC ASSOCIATION
BRAF
c-Raf
PTPN11
HEALTH SPECIALTY
cardiology
dermatology
rheumatology
Wikipedia
EN
Noonan Syndrome with Multiple Lentigines
Wikidata
EN
LEOPARD syndrome
Wikipedia Redirections
EN
Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome, Cardiocutaneous syndrome, Gorlin syndrome II, Gorlin syndrome type II, Lentiginosis profusa syndrome, LEOPARD syndrome, Moynahan syndrome, Multiple-lentigines (LEOPARD) syndrome, multiple lentigines syndrome, Noonan Syndrome with Multiple Lentigines, Noonan Syndrome with Multiple Lentigines (NSML) AKA Leopard Syndrome, progressive cardiomyopathic lentiginosis
Wikidata Alias
EN
Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome, Cardiocutaneous syndrome, Generalized lentiginosis, Gorlin syndrome II, Lentiginosis profusa syndrome, LEOPARD Syndrome, Moynahan syndrome, Multiple lentigines syndrome, Noonan syndrome with multiple lentigines, Progressive cardiomyopathic lentiginosis

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