ONKI3 | Medical Subject Headings

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The way concept relations are shown: separately in hierarchy

Langer-Giedion Syndrome

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Developmental ∟ Osteochondrodysplasias ∟ Langer-Giedion Syndrome 15 coordinate concepts ∟ Achondroplasia \| ∟ Acquired Hyperostosis Syndrome \| ∟ Camurati-Engelmann Syndrome \| ∟ Chondrodysplasia Punctata \| ∟ Cleidocranial Dysplasia \| ∟ Ellis-Van Creveld Syndrome \| ∟ Enchondromatosis \| ∟ Fibrous Dysplasia of Bone \| ∟ Hyperostosis Frontalis Interna \| ∟ Hyperostosis, Cortical, Congenital \| ∟ Osteochondroma \| ∟ Osteogenesis Imperfecta \| ∟ Osteosclerosis \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Thanatophoric Dysplasia X
Broader terms:	Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Developmental ∟ Osteochondrodysplasias ∟ Langer-Giedion Syndrome Osteochondrodysplasias > Bone Diseases, Developmental > Bone Diseases > Musculoskeletal Diseases > Medical Subject Headings (MeSH) X
Annotation:	an osteochondrodysplasia X
History note:	Exostoses, Multiple (1972-1989)X
historyNote*:	90; was GIEDION-LANGER SYNDROME see EXOSTOSES, MULTIPLE 1968-89 X
onlineNote*:	use EXOSTOSES, MULTIPLE to search GIEDION-LANGER SYNDROME 1968-89 X
publicMeSHNote*:	90; was GIEDION-LANGER SYNDROME see EXOSTOSES, MULTIPLE 1968-89 X
Scope note:	Autosomal dominant disorder characterized by cone-shaped epiphyses in the hands and multiple cartilaginous exostoses. Mental retardation and abnormalities of chromosome 8 are often present. The exostoses in this syndrome appear identical to those of hereditary multiple exostoses (EXOSTOSES, HEREDITARY MULTIPLE). X
activeMeSHYear*:	1991 \| 1992 \| 1993 \| 1994 \| 1995 \| 1996 \| 1997 \| 1998 \| 1999 \| 2000 \| 2001 \| 2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1989-05-15X
dateEstablished*:	1990-01-01X
dateRevised*:	1990-02-22X
recordAuthorizer*:	PLSX
recordMaintainer*:	PLSX
recordOriginator*:	AGSX
Type:	Concept X
Coordinate terms:	Achondroplasia \| Acquired Hyperostosis Syndrome \| Camurati-Engelmann Syndrome \| Chondrodysplasia Punctata \| Cleidocranial Dysplasia \| Ellis-Van Creveld Syndrome \| Enchondromatosis \| Fibrous Dysplasia of Bone \| Hyperostosis Frontalis Interna \| Hyperostosis, Cortical, Congenital \| Osteochondroma \| Osteogenesis Imperfecta \| Osteosclerosis \| Short Rib-Polydactyly Syndrome \| Thanatophoric Dysplasia X
URI:	X
Labels and equivalent concepts:	Langer-Giedion oireyhtymä (fi) Langer-Giedion syndrooma (fi, replaced) Langer-Giedions syndrom (sv) Trichorhinophalangeal Syndrome with Exostoses (en, replaced) Trichorhinophalangeal Syndrome Type II (en, replaced) Giedion-Langer Syndrome (en, replaced) Acrodysplasia V (en, replaced) Syndroma Langer-Giedion (la-FI, replaced) X
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