ONKI3 | Medical Subject Headings

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Peutz-Jeghers Syndrome

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Neoplastic Syndromes, Hereditary ∟ Peutz-Jeghers Syndrome 12 coordinate concepts ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Colorectal Neoplasms, Hereditary Nonpolyposis \| ∟ Dysplastic Nevus Syndrome \| ∟ Exostoses, Multiple Hereditary \| ∟ Hamartoma Syndrome, Multiple \| ∟ Li-Fraumeni Syndrome \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor \| ∟ LEOPARD Syndrome Medical Subject Headings (MeSH) ∟ Digestive System Diseases ∟ Gastrointestinal Diseases ∟ Intestinal Diseases ∟ Intestinal Polyposis ∟ Peutz-Jeghers Syndrome 12 coordinate concepts ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Colorectal Neoplasms, Hereditary Nonpolyposis \| ∟ Dysplastic Nevus Syndrome \| ∟ Exostoses, Multiple Hereditary \| ∟ Hamartoma Syndrome, Multiple \| ∟ Li-Fraumeni Syndrome \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor \| ∟ LEOPARD Syndrome Medical Subject Headings (MeSH) ∟ Neoplasms ∟ Neoplastic Syndromes, Hereditary ∟ Peutz-Jeghers Syndrome 12 coordinate concepts ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Colorectal Neoplasms, Hereditary Nonpolyposis \| ∟ Dysplastic Nevus Syndrome \| ∟ Exostoses, Multiple Hereditary \| ∟ Hamartoma Syndrome, Multiple \| ∟ Li-Fraumeni Syndrome \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor \| ∟ LEOPARD Syndrome Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Pigmentation Disorders ∟ Hyperpigmentation ∟ Melanosis ∟ Lentigo ∟ Peutz-Jeghers Syndrome 12 coordinate concepts ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Colorectal Neoplasms, Hereditary Nonpolyposis \| ∟ Dysplastic Nevus Syndrome \| ∟ Exostoses, Multiple Hereditary \| ∟ Hamartoma Syndrome, Multiple \| ∟ Li-Fraumeni Syndrome \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor \| ∟ LEOPARD Syndrome X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Neoplastic Syndromes, Hereditary ∟ Peutz-Jeghers Syndrome Medical Subject Headings (MeSH) ∟ Digestive System Diseases ∟ Gastrointestinal Diseases ∟ Intestinal Diseases ∟ Intestinal Polyposis ∟ Peutz-Jeghers Syndrome Medical Subject Headings (MeSH) ∟ Neoplasms ∟ Neoplastic Syndromes, Hereditary ∟ Peutz-Jeghers Syndrome Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Pigmentation Disorders ∟ Hyperpigmentation ∟ Melanosis ∟ Lentigo ∟ Peutz-Jeghers Syndrome Neoplastic Syndromes, Hereditary > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Intestinal Polyposis > Intestinal Diseases > Gastrointestinal Diseases > Digestive System Diseases > Medical Subject Headings (MeSH) Neoplastic Syndromes, Hereditary > Neoplasms > Medical Subject Headings (MeSH) Lentigo > Melanosis > Hyperpigmentation > Pigmentation Disorders > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) X
historyNote*:	65; was see under POLYPI (now POLYPS) 1963-64 X
publicMeSHNote*:	65; was see under POLYPI (now POLYPS) 1963-64 X
Scope note:	A hereditary disease caused by autosomal dominant mutations involving CHROMOSOME 19. It is characterized by the presence of INTESTINAL POLYPS, consistently in the JEJUNUM, and mucocutaneous pigmentation with MELANIN spots of the lips, buccal MUCOSA, and digits. X
activeMeSHYear*:	2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1965-01-01X
dateRevised*:	2003-07-09X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Adenomatous Polyposis Coli \| Basal Cell Nevus Syndrome \| Colorectal Neoplasms, Hereditary Nonpolyposis \| Dysplastic Nevus Syndrome \| Exostoses, Multiple Hereditary \| Hamartoma Syndrome, Multiple \| Li-Fraumeni Syndrome \| Multiple Endocrine Neoplasia \| Neurofibromatoses \| Sturge-Weber Syndrome \| Wilms Tumor \| LEOPARD Syndrome X
URI:	X
Labels and equivalent concepts:	Peutz-Jeghersin oireyhtymä (fi) Peutz-Jeghersin syndrooma (fi, replaced) Peutz-Jeghersin polypoosi (fi, replaced) Peutz-Jeghers syndrom (sv) Polyps-and-Spots Syndrome (en, replaced) Peutz-Jegher's Syndrome (en, replaced) Polyposis, Hamartomatous Intestinal (en, replaced) Lentiginosis, Perioral (en, replaced) Syndroma Peutz-Jeghers (la-FI, replaced) X
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