ONKI3 | Medical Subject Headings

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The way concept relations are shown: separately in hierarchy

Ellis-Van Creveld Syndrome

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Abnormalities, Multiple ∟ Ectodermal Dysplasia ∟ Ellis-Van Creveld Syndrome 21 coordinate concepts ∟ Achondroplasia \| ∟ Acquired Hyperostosis Syndrome \| ∟ Camurati-Engelmann Syndrome \| ∟ Chondrodysplasia Punctata \| ∟ Cleidocranial Dysplasia \| ∟ Enchondromatosis \| ∟ Fibrous Dysplasia of Bone \| ∟ Hyperostosis Frontalis Interna \| ∟ Hyperostosis, Cortical, Congenital \| ∟ Langer-Giedion Syndrome \| ∟ Osteochondroma \| ∟ Osteogenesis Imperfecta \| ∟ Osteosclerosis \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Thanatophoric Dysplasia \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Focal Dermal Hypoplasia \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Skin Abnormalities ∟ Ectodermal Dysplasia ∟ Ellis-Van Creveld Syndrome 21 coordinate concepts ∟ Achondroplasia \| ∟ Acquired Hyperostosis Syndrome \| ∟ Camurati-Engelmann Syndrome \| ∟ Chondrodysplasia Punctata \| ∟ Cleidocranial Dysplasia \| ∟ Enchondromatosis \| ∟ Fibrous Dysplasia of Bone \| ∟ Hyperostosis Frontalis Interna \| ∟ Hyperostosis, Cortical, Congenital \| ∟ Langer-Giedion Syndrome \| ∟ Osteochondroma \| ∟ Osteogenesis Imperfecta \| ∟ Osteosclerosis \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Thanatophoric Dysplasia \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Focal Dermal Hypoplasia \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Ectodermal Dysplasia ∟ Ellis-Van Creveld Syndrome 21 coordinate concepts ∟ Achondroplasia \| ∟ Acquired Hyperostosis Syndrome \| ∟ Camurati-Engelmann Syndrome \| ∟ Chondrodysplasia Punctata \| ∟ Cleidocranial Dysplasia \| ∟ Enchondromatosis \| ∟ Fibrous Dysplasia of Bone \| ∟ Hyperostosis Frontalis Interna \| ∟ Hyperostosis, Cortical, Congenital \| ∟ Langer-Giedion Syndrome \| ∟ Osteochondroma \| ∟ Osteogenesis Imperfecta \| ∟ Osteosclerosis \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Thanatophoric Dysplasia \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Focal Dermal Hypoplasia \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Developmental ∟ Osteochondrodysplasias ∟ Ellis-Van Creveld Syndrome 21 coordinate concepts ∟ Achondroplasia \| ∟ Acquired Hyperostosis Syndrome \| ∟ Camurati-Engelmann Syndrome \| ∟ Chondrodysplasia Punctata \| ∟ Cleidocranial Dysplasia \| ∟ Enchondromatosis \| ∟ Fibrous Dysplasia of Bone \| ∟ Hyperostosis Frontalis Interna \| ∟ Hyperostosis, Cortical, Congenital \| ∟ Langer-Giedion Syndrome \| ∟ Osteochondroma \| ∟ Osteogenesis Imperfecta \| ∟ Osteosclerosis \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Thanatophoric Dysplasia \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Focal Dermal Hypoplasia \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Abnormalities ∟ Ectodermal Dysplasia ∟ Ellis-Van Creveld Syndrome 21 coordinate concepts ∟ Achondroplasia \| ∟ Acquired Hyperostosis Syndrome \| ∟ Camurati-Engelmann Syndrome \| ∟ Chondrodysplasia Punctata \| ∟ Cleidocranial Dysplasia \| ∟ Enchondromatosis \| ∟ Fibrous Dysplasia of Bone \| ∟ Hyperostosis Frontalis Interna \| ∟ Hyperostosis, Cortical, Congenital \| ∟ Langer-Giedion Syndrome \| ∟ Osteochondroma \| ∟ Osteogenesis Imperfecta \| ∟ Osteosclerosis \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Thanatophoric Dysplasia \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Focal Dermal Hypoplasia \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Ectodermal Dysplasia ∟ Ellis-Van Creveld Syndrome 21 coordinate concepts ∟ Achondroplasia \| ∟ Acquired Hyperostosis Syndrome \| ∟ Camurati-Engelmann Syndrome \| ∟ Chondrodysplasia Punctata \| ∟ Cleidocranial Dysplasia \| ∟ Enchondromatosis \| ∟ Fibrous Dysplasia of Bone \| ∟ Hyperostosis Frontalis Interna \| ∟ Hyperostosis, Cortical, Congenital \| ∟ Langer-Giedion Syndrome \| ∟ Osteochondroma \| ∟ Osteogenesis Imperfecta \| ∟ Osteosclerosis \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Thanatophoric Dysplasia \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Focal Dermal Hypoplasia \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Abnormalities, Multiple ∟ Ectodermal Dysplasia ∟ Ellis-Van Creveld Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Skin Abnormalities ∟ Ectodermal Dysplasia ∟ Ellis-Van Creveld Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Ectodermal Dysplasia ∟ Ellis-Van Creveld Syndrome Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Developmental ∟ Osteochondrodysplasias ∟ Ellis-Van Creveld Syndrome Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Abnormalities ∟ Ectodermal Dysplasia ∟ Ellis-Van Creveld Syndrome Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Ectodermal Dysplasia ∟ Ellis-Van Creveld Syndrome Ectodermal Dysplasia > Abnormalities, Multiple > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Ectodermal Dysplasia > Skin Abnormalities > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Ectodermal Dysplasia > Skin Diseases, Genetic > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Osteochondrodysplasias > Bone Diseases, Developmental > Bone Diseases > Musculoskeletal Diseases > Medical Subject Headings (MeSH) Ectodermal Dysplasia > Skin Abnormalities > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) Ectodermal Dysplasia > Skin Diseases, Genetic > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) X
Annotation:	do not use /congen & do not coord with INFANT, NEWBORN, DISEASES X
historyNote*:	65(63) X
publicMeSHNote*:	65 X
Scope note:	Dwarfism occurring in association with defective development of skin, hair, and teeth, polydactyly, and defect of the cardiac septum. (Dorland, 27th ed) X
activeMeSHYear*:	2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1965-01-01X
dateRevised*:	2001-07-25X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Achondroplasia \| Acquired Hyperostosis Syndrome \| Camurati-Engelmann Syndrome \| Chondrodysplasia Punctata \| Cleidocranial Dysplasia \| Enchondromatosis \| Fibrous Dysplasia of Bone \| Hyperostosis Frontalis Interna \| Hyperostosis, Cortical, Congenital \| Langer-Giedion Syndrome \| Osteochondroma \| Osteogenesis Imperfecta \| Osteosclerosis \| Short Rib-Polydactyly Syndrome \| Thanatophoric Dysplasia \| Ectodermal Dysplasia 1, Anhidrotic \| Ectodermal Dysplasia 3, Anhidrotic \| Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| Focal Dermal Hypoplasia \| Neurocutaneous Syndromes \| Pachyonychia Congenita X
URI:	X
Labels and equivalent concepts:	Kondroektodermaalinen dysplasia (fi) Ellis-Van Creveldin syndrooma (fi, replaced) Ellis-Van Creveldin oireyhtymä (fi, replaced) Ellis-Van Crevelds syndrom (sv) Chondroectodermal Dysplasia (en, replaced) Syndroma Ellis-Van Creveld (la-FI, replaced) Dysplasia chondroectodermalis (la-FI, replaced) X
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