ONKI3 | Medical Subject Headings

The ONKI is provided as a part of the ONKI Living Lab - an open lab for testing the latest semantic web technologies in practice, with real users like you. Currently, over 10 000 people are using ONKI each month.

We hope you like the ONKI service and enjoy using it for your purposes!

If you encounter any problems or have improvement ideas, please contact the ONKI team. We are also very much interested in your success stories in using ONKI - please share your experiences!

The ONKI Team

Jouni Tuominen, Living Lab contact person, APIs, widgets, publishing of ontologies, etc.
Eero Hyvönen, professor, head of research group

Former members: Kim Viljanen, Rami Alatalo.

Building the future of the Semantic Web and beyond.

SeCo's homepage
For the latest semantic news, follow us on Twitter and fan us on Facebook!

How can we help you?

Live presentations about ONKI: what it is? how to use it?
Support for creating and publishing ontologies.
Online technical support for using ONKI.
Co-operation in projects.
And more, please ask.

suomeksi på svenska in English

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

The way concept relations are shown: separately in hierarchy

Hamartoma Syndrome, Multiple

Loading results...


Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Neoplastic Syndromes, Hereditary ∟ Hamartoma Syndrome, Multiple 13 coordinate concepts ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Colorectal Neoplasms, Hereditary Nonpolyposis \| ∟ Dysplastic Nevus Syndrome \| ∟ Exostoses, Multiple Hereditary \| ∟ Li-Fraumeni Syndrome \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Peutz-Jeghers Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor \| ∟ Proteus Syndrome \| ∟ Tuberous Sclerosis Medical Subject Headings (MeSH) ∟ Neoplasms ∟ Hamartoma ∟ Hamartoma Syndrome, Multiple 13 coordinate concepts ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Colorectal Neoplasms, Hereditary Nonpolyposis \| ∟ Dysplastic Nevus Syndrome \| ∟ Exostoses, Multiple Hereditary \| ∟ Li-Fraumeni Syndrome \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Peutz-Jeghers Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor \| ∟ Proteus Syndrome \| ∟ Tuberous Sclerosis Medical Subject Headings (MeSH) ∟ Neoplasms ∟ Neoplasms, Multiple Primary ∟ Hamartoma Syndrome, Multiple 13 coordinate concepts ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Colorectal Neoplasms, Hereditary Nonpolyposis \| ∟ Dysplastic Nevus Syndrome \| ∟ Exostoses, Multiple Hereditary \| ∟ Li-Fraumeni Syndrome \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Peutz-Jeghers Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor \| ∟ Proteus Syndrome \| ∟ Tuberous Sclerosis Medical Subject Headings (MeSH) ∟ Neoplasms ∟ Neoplastic Syndromes, Hereditary ∟ Hamartoma Syndrome, Multiple 13 coordinate concepts ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Colorectal Neoplasms, Hereditary Nonpolyposis \| ∟ Dysplastic Nevus Syndrome \| ∟ Exostoses, Multiple Hereditary \| ∟ Li-Fraumeni Syndrome \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Peutz-Jeghers Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor \| ∟ Proteus Syndrome \| ∟ Tuberous Sclerosis X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Neoplastic Syndromes, Hereditary ∟ Hamartoma Syndrome, Multiple Medical Subject Headings (MeSH) ∟ Neoplasms ∟ Hamartoma ∟ Hamartoma Syndrome, Multiple Medical Subject Headings (MeSH) ∟ Neoplasms ∟ Neoplasms, Multiple Primary ∟ Hamartoma Syndrome, Multiple Medical Subject Headings (MeSH) ∟ Neoplasms ∟ Neoplastic Syndromes, Hereditary ∟ Hamartoma Syndrome, Multiple Neoplastic Syndromes, Hereditary > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Hamartoma > Neoplasms > Medical Subject Headings (MeSH) Neoplasms, Multiple Primary > Neoplasms > Medical Subject Headings (MeSH) Neoplastic Syndromes, Hereditary > Neoplasms > Medical Subject Headings (MeSH) X
Annotation:	do not use /blood supply /chem /second /secret /ultrastruct X
History note:	Hamartoma (1966-1986) \| Neoplasms, Multiple Primary (1966-1986)X
historyNote*:	91(87); was see under NEOPLASMS, MULTIPLE PRIMARY 1987-90 X
publicMeSHNote*:	91; was see under NEOPLASMS, MULTIPLE PRIMARY 1987-90 X
Scope note:	A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Papules of the face and oral mucosa are the most characteristic lesion. Other changes occur in the skin, in the thyroid, the breast, the gastrointestinal system, and the nervous system. X
activeMeSHYear*:	2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1986-06-23X
dateEstablished*:	1991-01-01X
dateRevised*:	2001-07-25X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	VDKX
Type:	Concept X
Coordinate terms:	Adenomatous Polyposis Coli \| Basal Cell Nevus Syndrome \| Colorectal Neoplasms, Hereditary Nonpolyposis \| Dysplastic Nevus Syndrome \| Exostoses, Multiple Hereditary \| Li-Fraumeni Syndrome \| Multiple Endocrine Neoplasia \| Neurofibromatoses \| Peutz-Jeghers Syndrome \| Sturge-Weber Syndrome \| Wilms Tumor \| Proteus Syndrome \| Tuberous Sclerosis X
URI:	X
Labels and equivalent concepts:	Multippeli hamartooma -oireyhtymä (fi) Multippeli hamartooma -syndrooma (fi, replaced) Cowdenin tauti (fi, replaced) Hamartomsyndrom, multipelt (sv) Multipelt hamartomsyndrom (sv, replaced) Cowden's Disease (en, replaced) Multiple Hamartoma Syndrome (en, replaced) Cowden Disease (en, replaced) Morbus Cowden (la-FI, replaced) X
Share:	X