ONKI3 | MedIEQ: Medical Subject Headings

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The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

Colorectal Neoplasms, Hereditary Nonpolyposis

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Neoplastic Syndromes, Hereditary ∟ Colorectal Neoplasms, Hereditary Nonpolyposis 22 coordinate concepts ∟ Ataxia Telangiectasia \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Fanconi Anemia \| ∟ Li-Fraumeni Syndrome \| ∟ Nijmegen Breakage Syndrome \| ∟ Rothmund-Thomson Syndrome \| ∟ Severe Combined Immunodeficiency \| ∟ Werner Syndrome \| ∟ Xeroderma Pigmentosum \| ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Dysplastic Nevus Syndrome \| ∟ Exostoses, Multiple Hereditary \| ∟ Hamartoma Syndrome, Multiple \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Peutz-Jeghers Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor \| ∟ Colonic Neoplasms \| ∟ Rectal Neoplasms Medical Subject Headings (MeSH) ∟ Digestive System Diseases ∟ Digestive System Neoplasms ∟ Gastrointestinal Neoplasms ∟ Intestinal Neoplasms ∟ Colorectal Neoplasms ∟ Colorectal Neoplasms, Hereditary Nonpolyposis 22 coordinate concepts ∟ Ataxia Telangiectasia \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Fanconi Anemia \| ∟ Li-Fraumeni Syndrome \| ∟ Nijmegen Breakage Syndrome \| ∟ Rothmund-Thomson Syndrome \| ∟ Severe Combined Immunodeficiency \| ∟ Werner Syndrome \| ∟ Xeroderma Pigmentosum \| ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Dysplastic Nevus Syndrome \| ∟ Exostoses, Multiple Hereditary \| ∟ Hamartoma Syndrome, Multiple \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Peutz-Jeghers Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor \| ∟ Colonic Neoplasms \| ∟ Rectal Neoplasms Medical Subject Headings (MeSH) ∟ Digestive System Diseases ∟ Gastrointestinal Diseases ∟ Gastrointestinal Neoplasms ∟ Intestinal Neoplasms ∟ Colorectal Neoplasms ∟ Colorectal Neoplasms, Hereditary Nonpolyposis 22 coordinate concepts ∟ Ataxia Telangiectasia \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Fanconi Anemia \| ∟ Li-Fraumeni Syndrome \| ∟ Nijmegen Breakage Syndrome \| ∟ Rothmund-Thomson Syndrome \| ∟ Severe Combined Immunodeficiency \| ∟ Werner Syndrome \| ∟ Xeroderma Pigmentosum \| ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Dysplastic Nevus Syndrome \| ∟ Exostoses, Multiple Hereditary \| ∟ Hamartoma Syndrome, Multiple \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Peutz-Jeghers Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor \| ∟ Colonic Neoplasms \| ∟ Rectal Neoplasms Medical Subject Headings (MeSH) ∟ Digestive System Diseases ∟ Gastrointestinal Diseases ∟ Intestinal Diseases ∟ Colonic Diseases ∟ Colorectal Neoplasms ∟ Colorectal Neoplasms, Hereditary Nonpolyposis 22 coordinate concepts ∟ Ataxia Telangiectasia \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Fanconi Anemia \| ∟ Li-Fraumeni Syndrome \| ∟ Nijmegen Breakage Syndrome \| ∟ Rothmund-Thomson Syndrome \| ∟ Severe Combined Immunodeficiency \| ∟ Werner Syndrome \| ∟ Xeroderma Pigmentosum \| ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Dysplastic Nevus Syndrome \| ∟ Exostoses, Multiple Hereditary \| ∟ Hamartoma Syndrome, Multiple \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Peutz-Jeghers Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor \| ∟ Colonic Neoplasms \| ∟ Rectal Neoplasms Medical Subject Headings (MeSH) ∟ Digestive System Diseases ∟ Gastrointestinal Diseases ∟ Intestinal Diseases ∟ Intestinal Neoplasms ∟ Colorectal Neoplasms ∟ Colorectal Neoplasms, Hereditary Nonpolyposis 22 coordinate concepts ∟ Ataxia Telangiectasia \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Fanconi Anemia \| ∟ Li-Fraumeni Syndrome \| ∟ Nijmegen Breakage Syndrome \| ∟ Rothmund-Thomson Syndrome \| ∟ Severe Combined Immunodeficiency \| ∟ Werner Syndrome \| ∟ Xeroderma Pigmentosum \| ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Dysplastic Nevus Syndrome \| ∟ Exostoses, Multiple Hereditary \| ∟ Hamartoma Syndrome, Multiple \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Peutz-Jeghers Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor \| ∟ Colonic Neoplasms \| ∟ Rectal Neoplasms Medical Subject Headings (MeSH) ∟ Digestive System Diseases ∟ Gastrointestinal Diseases ∟ Intestinal Diseases ∟ Rectal Diseases ∟ Colorectal Neoplasms ∟ Colorectal Neoplasms, Hereditary Nonpolyposis 22 coordinate concepts ∟ Ataxia Telangiectasia \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Fanconi Anemia \| ∟ Li-Fraumeni Syndrome \| ∟ Nijmegen Breakage Syndrome \| ∟ Rothmund-Thomson Syndrome \| ∟ Severe Combined Immunodeficiency \| ∟ Werner Syndrome \| ∟ Xeroderma Pigmentosum \| ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Dysplastic Nevus Syndrome \| ∟ Exostoses, Multiple Hereditary \| ∟ Hamartoma Syndrome, Multiple \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Peutz-Jeghers Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor \| ∟ Colonic Neoplasms \| ∟ Rectal Neoplasms Medical Subject Headings (MeSH) ∟ Neoplasms ∟ Neoplasms by Site ∟ Digestive System Neoplasms ∟ Gastrointestinal Neoplasms ∟ Intestinal Neoplasms ∟ Colorectal Neoplasms ∟ Colorectal Neoplasms, Hereditary Nonpolyposis 22 coordinate concepts ∟ Ataxia Telangiectasia \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Fanconi Anemia \| ∟ Li-Fraumeni Syndrome \| ∟ Nijmegen Breakage Syndrome \| ∟ Rothmund-Thomson Syndrome \| ∟ Severe Combined Immunodeficiency \| ∟ Werner Syndrome \| ∟ Xeroderma Pigmentosum \| ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Dysplastic Nevus Syndrome \| ∟ Exostoses, Multiple Hereditary \| ∟ Hamartoma Syndrome, Multiple \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Peutz-Jeghers Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor \| ∟ Colonic Neoplasms \| ∟ Rectal Neoplasms Medical Subject Headings (MeSH) ∟ Neoplasms ∟ Neoplastic Syndromes, Hereditary ∟ Colorectal Neoplasms, Hereditary Nonpolyposis 22 coordinate concepts ∟ Ataxia Telangiectasia \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Fanconi Anemia \| ∟ Li-Fraumeni Syndrome \| ∟ Nijmegen Breakage Syndrome \| ∟ Rothmund-Thomson Syndrome \| ∟ Severe Combined Immunodeficiency \| ∟ Werner Syndrome \| ∟ Xeroderma Pigmentosum \| ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Dysplastic Nevus Syndrome \| ∟ Exostoses, Multiple Hereditary \| ∟ Hamartoma Syndrome, Multiple \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Peutz-Jeghers Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor \| ∟ Colonic Neoplasms \| ∟ Rectal Neoplasms Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ DNA Repair-Deficiency Disorders ∟ Colorectal Neoplasms, Hereditary Nonpolyposis 22 coordinate concepts ∟ Ataxia Telangiectasia \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Fanconi Anemia \| ∟ Li-Fraumeni Syndrome \| ∟ Nijmegen Breakage Syndrome \| ∟ Rothmund-Thomson Syndrome \| ∟ Severe Combined Immunodeficiency \| ∟ Werner Syndrome \| ∟ Xeroderma Pigmentosum \| ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Dysplastic Nevus Syndrome \| ∟ Exostoses, Multiple Hereditary \| ∟ Hamartoma Syndrome, Multiple \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Peutz-Jeghers Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor \| ∟ Colonic Neoplasms \| ∟ Rectal Neoplasms X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Neoplastic Syndromes, Hereditary ∟ Colorectal Neoplasms, Hereditary Nonpolyposis Medical Subject Headings (MeSH) ∟ Digestive System Diseases ∟ Digestive System Neoplasms ∟ Gastrointestinal Neoplasms ∟ Intestinal Neoplasms ∟ Colorectal Neoplasms ∟ Colorectal Neoplasms, Hereditary Nonpolyposis Medical Subject Headings (MeSH) ∟ Digestive System Diseases ∟ Gastrointestinal Diseases ∟ Gastrointestinal Neoplasms ∟ Intestinal Neoplasms ∟ Colorectal Neoplasms ∟ Colorectal Neoplasms, Hereditary Nonpolyposis Medical Subject Headings (MeSH) ∟ Digestive System Diseases ∟ Gastrointestinal Diseases ∟ Intestinal Diseases ∟ Colonic Diseases ∟ Colorectal Neoplasms ∟ Colorectal Neoplasms, Hereditary Nonpolyposis Medical Subject Headings (MeSH) ∟ Digestive System Diseases ∟ Gastrointestinal Diseases ∟ Intestinal Diseases ∟ Intestinal Neoplasms ∟ Colorectal Neoplasms ∟ Colorectal Neoplasms, Hereditary Nonpolyposis Medical Subject Headings (MeSH) ∟ Digestive System Diseases ∟ Gastrointestinal Diseases ∟ Intestinal Diseases ∟ Rectal Diseases ∟ Colorectal Neoplasms ∟ Colorectal Neoplasms, Hereditary Nonpolyposis Medical Subject Headings (MeSH) ∟ Neoplasms ∟ Neoplasms by Site ∟ Digestive System Neoplasms ∟ Gastrointestinal Neoplasms ∟ Intestinal Neoplasms ∟ Colorectal Neoplasms ∟ Colorectal Neoplasms, Hereditary Nonpolyposis Medical Subject Headings (MeSH) ∟ Neoplasms ∟ Neoplastic Syndromes, Hereditary ∟ Colorectal Neoplasms, Hereditary Nonpolyposis Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ DNA Repair-Deficiency Disorders ∟ Colorectal Neoplasms, Hereditary Nonpolyposis Neoplastic Syndromes, Hereditary > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Colorectal Neoplasms > Intestinal Neoplasms > Gastrointestinal Neoplasms > Digestive System Neoplasms > Digestive System Diseases > Medical Subject Headings (MeSH) Colorectal Neoplasms > Intestinal Neoplasms > Gastrointestinal Neoplasms > Gastrointestinal Diseases > Digestive System Diseases > Medical Subject Headings (MeSH) Colorectal Neoplasms > Colonic Diseases > Intestinal Diseases > Gastrointestinal Diseases > Digestive System Diseases > Medical Subject Headings (MeSH) Colorectal Neoplasms > Intestinal Neoplasms > Intestinal Diseases > Gastrointestinal Diseases > Digestive System Diseases > Medical Subject Headings (MeSH) Colorectal Neoplasms > Rectal Diseases > Intestinal Diseases > Gastrointestinal Diseases > Digestive System Diseases > Medical Subject Headings (MeSH) Colorectal Neoplasms > Intestinal Neoplasms > Gastrointestinal Neoplasms > Digestive System Neoplasms > Neoplasms by Site > Neoplasms > Medical Subject Headings (MeSH) Neoplastic Syndromes, Hereditary > Neoplasms > Medical Subject Headings (MeSH) DNA Repair-Deficiency Disorders > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) X
Annotation:	DF: HNPCC X
historyNote*:	87 X
publicMeSHNote*:	87 X
Scope note:	A group of autosomal-dominant inherited diseases in which COLON CANCER arises in discrete adenomas. Unlike FAMILIAL POLYPOSIS COLI with hundreds of polyps, hereditary nonpolyposis colorectal neoplasms occur much later, in the fourth and fifth decades. HNPCC has been associated with germline mutations in mismatch repair (MMR) genes. X
activeMeSHYear*:	2006 \| 2007X
dateCreated*:	1986-06-24X
dateEstablished*:	1987-01-01X
dateRevised*:	2005-06-30X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	VDKX
Type:	Concept X
Coordinate terms:	Ataxia Telangiectasia \| Bloom Syndrome \| Cockayne Syndrome \| Fanconi Anemia \| Li-Fraumeni Syndrome \| Nijmegen Breakage Syndrome \| Rothmund-Thomson Syndrome \| Severe Combined Immunodeficiency \| Werner Syndrome \| Xeroderma Pigmentosum \| Adenomatous Polyposis Coli \| Basal Cell Nevus Syndrome \| Dysplastic Nevus Syndrome \| Exostoses, Multiple Hereditary \| Hamartoma Syndrome, Multiple \| Multiple Endocrine Neoplasia \| Neurofibromatoses \| Peutz-Jeghers Syndrome \| Sturge-Weber Syndrome \| Wilms Tumor \| Colonic Neoplasms \| Rectal Neoplasms X
URI:	X
Labels and equivalent concepts:	Periytyvä ei-polypoottinen paksusuolisyöpä (fi) Lynch Syndrome I (en, replaced) Lynch Syndrome (en, replaced) Lynch Cancer Family Syndrome I (en, replaced) Hereditary Nonpolyposis Colorectal Neoplasms (en, replaced) Colon Cancer, Familial Nonpolyposis (en, replaced) Neoplasias Colorrectales Hereditarias sin Poliposis (es) κληρονομικά μη πολυποδικά ορθοκολπικά νεοπλάσματα (el) Kolorektale Tumoren, hereditäre, ohne Polypose (de) kolorektální nádory dědičné nepolypózní (cs) Cáncer Colorrectal Hereditario sin Poliposis (es, replaced) Neoplasias Colorrectales no Poliposis Hereditarios (es, replaced) Síndrome de Lynch (es, replaced) Erbliche nichtpolypöse kolorektale Tumoren (de, replaced) Lynchův syndrom II (cs, replaced) Hereditärer nichtpolypöser kolorektaler bösartiger Tumor (de, replaced) Lynch-Syndrom II (de, replaced) hereditární nepolypózní kolorektální karcinom (cs, replaced) X
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