Noonan syndrome with multiple lentigines
Noonan syndrome with multiple lentigines (NSML) 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 (PTPN11). The disease is a complex of features, mostly involving the skin, skeletal and cardiovascular systems, which may or may not be present in all patients. The nature of how the mutation causes each of the condition's symptoms is not well known; however, research is ongoing. It is a RASopathy.
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Cardiocutaneous syndromeGorlin syndrome IIGorlin syndrome type IILEOPARD syndromeLentiginosis profusa syndromeLeopard syndromeMoynahan syndromeMultiple-lentigines (LEOPARD) syndromeMultiple lentigines syndromeNoonan Syndrome with Multiple LentiginesNoonan Syndrome with Multiple Lentigines (NSML) AKA Leopard SyndromeProgressive cardiomyopathic lentiginosis
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1,2-dimethoxyethaanCardiocutaneous syndromeCongenital heart defectGeneralized lentiginosisGorlin syndrome IIGorlin syndrome type IIGranular cell tumorHypertelorismInterdigital webbingLEOPARD syndromeLentiginosisLentiginosis profusa syndromeLentigoLeopard (disambiguation)Leopard syndromeList of MeSH codes (C05)List of MeSH codes (C14)List of MeSH codes (C16)List of MeSH codes (C17)List of OMIM disorder codesList of genes mutated in cutaneous conditionsList of skin conditionsList of syndromesLow-set earsMoynahanMoynahan syndromeMultiple-lentigines (LEOPARD) syndromeMultiple lentigines syndromeNeuro-cardio-facial-cutaneous syndromesNeurofibromatosisNoonan Syndrome with Multiple LentiginesNoonan Syndrome with Multiple Lentigines (NSML) AKA Leopard SyndromePTPN11Pectus carinatumProgressive cardiomyopathic lentiginosisProtein tyrosine phosphataseRASopathySyndromes affecting the heart
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Noonan syndrome with multiple lentigines
Noonan syndrome with multiple lentigines (NSML) 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 (PTPN11). The disease is a complex of features, mostly involving the skin, skeletal and cardiovascular systems, which may or may not be present in all patients. The nature of how the mutation causes each of the condition's symptoms is not well known; however, research is ongoing. It is a RASopathy.
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Das LEOPARD-Syndrom bezeichnet ...... yndroms erfolgt symptomatisch.
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El síndrome LEOPARD, también l ...... ndividualizada en el año 1961.
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La sindrome LEOPARD, o lentigg ...... la presenza delle lentiggini.
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La síndrome LEOPARD (també con ...... giques de la síndrome LEOPARD.
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Le syndrome LEOPARD est une ma ...... s (en anglais) de ce syndrome.
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Noonan syndrome with multiple ...... ological data exists for NSML.
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Zespół LEOPARD (ang. LEOPARD s ...... stępować kilka z tych objawów.
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متلازمة نونان ذات الصبغيات الم ...... ة نونان ذات التصبغات المتعددة.
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1096445
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geneReviewsName
LEOPARD Syndrome
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997,345,118
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Three-quarter facial view, fir ...... t prognathism and low set ears
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DiseasesDB
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eMedicineTopic
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LEOPARD Syndrome
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NBK1383
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Noonan syndrome with multiple lentigines
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LEOPARD syndrome, cardiocutane ...... on syndrome, Moynahan syndrome
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Das LEOPARD-Syndrom bezeichnet ...... LEOPARD als Akronym steht für:
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El síndrome LEOPARD, también l ...... ndividualizada en el año 1961.
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La sindrome LEOPARD, o lentigg ...... la presenza delle lentiggini.
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La síndrome LEOPARD (també con ...... la investigació està en curs.
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Le syndrome LEOPARD est une ma ...... s (en anglais) de ce syndrome.
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Noonan syndrome with multiple ...... is ongoing. It is a RASopathy.
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Zespół LEOPARD (ang. LEOPARD s ...... . U jednego pacjenta może wyst
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متلازمة نونان ذات الصبغيات الم ...... وبالنظر إلى الإحصائيات، تعتبر
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label
LEOPARD-Syndrom
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Noonan syndrome with multiple lentigines
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Sindrome LEOPARD
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Syndrome LEOPARD
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Síndrome LEOPARD
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Síndrome LEOPARD
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Zespół LEOPARD
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متلازمة نونان ذات التصبغات المتعددة
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Noonan syndrome with multiple lentigines (NSML)
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