ONKI3 | 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

Exostoses, Multiple Hereditary

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Neoplastic Syndromes, Hereditary ∟ Exostoses, Multiple Hereditary 12 coordinate concepts ∟ Heel Spur \| ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Colorectal Neoplasms, Hereditary Nonpolyposis \| ∟ Dysplastic Nevus Syndrome \| ∟ Hamartoma Syndrome, Multiple \| ∟ Li-Fraumeni Syndrome \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Peutz-Jeghers Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Developmental ∟ Osteochondrodysplasias ∟ Osteochondroma ∟ Osteochondromatosis ∟ Exostoses, Multiple Hereditary 12 coordinate concepts ∟ Heel Spur \| ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Colorectal Neoplasms, Hereditary Nonpolyposis \| ∟ Dysplastic Nevus Syndrome \| ∟ Hamartoma Syndrome, Multiple \| ∟ Li-Fraumeni Syndrome \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Peutz-Jeghers Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Hyperostosis ∟ Exostoses ∟ Exostoses, Multiple Hereditary 12 coordinate concepts ∟ Heel Spur \| ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Colorectal Neoplasms, Hereditary Nonpolyposis \| ∟ Dysplastic Nevus Syndrome \| ∟ Hamartoma Syndrome, Multiple \| ∟ Li-Fraumeni Syndrome \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Peutz-Jeghers Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor Medical Subject Headings (MeSH) ∟ Neoplasms ∟ Neoplasms by Histologic Type ∟ Neoplasms, Connective and Soft Tissue ∟ Neoplasms, Connective Tissue ∟ Neoplasms, Bone Tissue ∟ Osteochondroma ∟ Osteochondromatosis ∟ Exostoses, Multiple Hereditary 12 coordinate concepts ∟ Heel Spur \| ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Colorectal Neoplasms, Hereditary Nonpolyposis \| ∟ Dysplastic Nevus Syndrome \| ∟ Hamartoma Syndrome, Multiple \| ∟ Li-Fraumeni Syndrome \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Peutz-Jeghers Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor Medical Subject Headings (MeSH) ∟ Neoplasms ∟ Neoplastic Syndromes, Hereditary ∟ Exostoses, Multiple Hereditary 12 coordinate concepts ∟ Heel Spur \| ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Colorectal Neoplasms, Hereditary Nonpolyposis \| ∟ Dysplastic Nevus Syndrome \| ∟ Hamartoma Syndrome, Multiple \| ∟ Li-Fraumeni Syndrome \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Peutz-Jeghers Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Connective Tissue Diseases ∟ Neoplasms, Connective Tissue ∟ Neoplasms, Bone Tissue ∟ Osteochondroma ∟ Osteochondromatosis ∟ Exostoses, Multiple Hereditary 12 coordinate concepts ∟ Heel Spur \| ∟ Adenomatous Polyposis Coli \| ∟ Basal Cell Nevus Syndrome \| ∟ Colorectal Neoplasms, Hereditary Nonpolyposis \| ∟ Dysplastic Nevus Syndrome \| ∟ Hamartoma Syndrome, Multiple \| ∟ Li-Fraumeni Syndrome \| ∟ Multiple Endocrine Neoplasia \| ∟ Neurofibromatoses \| ∟ Peutz-Jeghers Syndrome \| ∟ Sturge-Weber Syndrome \| ∟ Wilms Tumor X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Neoplastic Syndromes, Hereditary ∟ Exostoses, Multiple Hereditary Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Developmental ∟ Osteochondrodysplasias ∟ Osteochondroma ∟ Osteochondromatosis ∟ Exostoses, Multiple Hereditary Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Hyperostosis ∟ Exostoses ∟ Exostoses, Multiple Hereditary Medical Subject Headings (MeSH) ∟ Neoplasms ∟ Neoplasms by Histologic Type ∟ Neoplasms, Connective and Soft Tissue ∟ Neoplasms, Connective Tissue ∟ Neoplasms, Bone Tissue ∟ Osteochondroma ∟ Osteochondromatosis ∟ Exostoses, Multiple Hereditary Medical Subject Headings (MeSH) ∟ Neoplasms ∟ Neoplastic Syndromes, Hereditary ∟ Exostoses, Multiple Hereditary Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Connective Tissue Diseases ∟ Neoplasms, Connective Tissue ∟ Neoplasms, Bone Tissue ∟ Osteochondroma ∟ Osteochondromatosis ∟ Exostoses, Multiple Hereditary Neoplastic Syndromes, Hereditary > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Osteochondromatosis > Osteochondroma > Osteochondrodysplasias > Bone Diseases, Developmental > Bone Diseases > Musculoskeletal Diseases > Medical Subject Headings (MeSH) Exostoses > Hyperostosis > Bone Diseases > Musculoskeletal Diseases > Medical Subject Headings (MeSH) Osteochondromatosis > Osteochondroma > Neoplasms, Bone Tissue > Neoplasms, Connective Tissue > Neoplasms, Connective and Soft Tissue > Neoplasms by Histologic Type > Neoplasms > Medical Subject Headings (MeSH) Neoplastic Syndromes, Hereditary > Neoplasms > Medical Subject Headings (MeSH) Osteochondromatosis > Osteochondroma > Neoplasms, Bone Tissue > Neoplasms, Connective Tissue > Connective Tissue Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) X
History note:	Exostoses (1966-1967)X
historyNote*:	90; was EXOSTOSES, MULTIPLE 1968-89 X
onlineNote*:	use EXOSTOSES, MULTIPLE HEREDITARY to search EXOSTOSES, MULTIPLE 1968-89 X
publicMeSHNote*:	90; was EXOSTOSES, MULTIPLE 1968-89 X
Scope note:	Hereditary disorder transmitted by an autosomal dominant gene and characterized by multiple exostoses (multiple osteochondromas) near the ends of long bones. The genetic abnormality results in a defect in the osteoclastic activity at the metaphyseal ends of the bone during the remodeling process in childhood or early adolescence. The metaphyses develop benign, bony outgrowths often capped by cartilage. A small number undergo neoplastic transformation. X
activeMeSHYear*:	2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1968-01-01X
dateRevised*:	2001-07-25X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Heel Spur \| Adenomatous Polyposis Coli \| Basal Cell Nevus Syndrome \| Colorectal Neoplasms, Hereditary Nonpolyposis \| Dysplastic Nevus Syndrome \| Hamartoma Syndrome, Multiple \| Li-Fraumeni Syndrome \| Multiple Endocrine Neoplasia \| Neurofibromatoses \| Peutz-Jeghers Syndrome \| Sturge-Weber Syndrome \| Wilms Tumor X
URI:	X
Labels and equivalent concepts:	Perinnöllinen eksostoositauti (fi) Multippelit perinnölliset eksostoosit (fi, replaced) Multippelit hereditaariset eksostoosit (fi, replaced) Diafyseaalinen aklasia (fi, replaced) Multippelit periytyvät eksostoosit (fi, replaced) Useat synnynnäiset eksostoosit (fi, replaced) Exostoser, multipla ärftliga (sv) Ärftliga multipla exostoser (sv, replaced) Osteochondromas, Multiple (en, replaced) Hereditary Multiple Exostosis (en, replaced) Hereditary Multiple Exostoses (en, replaced) Exostoses, Multiple (en, replaced) Exostoses, Hereditary Multiple (en, replaced) Exostoses, Familial (en, replaced) Diaphyseal Aclasis (en, replaced) Exostoses, Multiple Cartilaginous (en, replaced) Exostosis, Familial (en, replaced) Exostosis, Multiple Cartilaginous (en, replaced) Exostosis, Multiple (en, replaced) Exostosis, Hereditary Multiple (en, replaced) Chondrodysplasia, Hereditary Deforming (en, replaced) Exostoses congenitae multiplices (la-FI, replaced) Aclasis diaphysialis (la-FI, replaced) X
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