ONKI3 | Medical Subject Headings

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Camurati-Engelmann Syndrome

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Camurati-Engelmann Syndrome 48 coordinate concepts ∟ Achondroplasia \| ∟ Acquired Hyperostosis Syndrome \| ∟ Chondrodysplasia Punctata \| ∟ Cleidocranial Dysplasia \| ∟ Ellis-Van Creveld Syndrome \| ∟ Enchondromatosis \| ∟ Fibrous Dysplasia of Bone \| ∟ Hyperostosis Frontalis Interna \| ∟ Hyperostosis, Cortical, Congenital \| ∟ Langer-Giedion Syndrome \| ∟ Osteochondroma \| ∟ Osteogenesis Imperfecta \| ∟ Osteosclerosis \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Thanatophoric Dysplasia \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ CADASIL \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Developmental ∟ Osteochondrodysplasias ∟ Camurati-Engelmann Syndrome 48 coordinate concepts ∟ Achondroplasia \| ∟ Acquired Hyperostosis Syndrome \| ∟ Chondrodysplasia Punctata \| ∟ Cleidocranial Dysplasia \| ∟ Ellis-Van Creveld Syndrome \| ∟ Enchondromatosis \| ∟ Fibrous Dysplasia of Bone \| ∟ Hyperostosis Frontalis Interna \| ∟ Hyperostosis, Cortical, Congenital \| ∟ Langer-Giedion Syndrome \| ∟ Osteochondroma \| ∟ Osteogenesis Imperfecta \| ∟ Osteosclerosis \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Thanatophoric Dysplasia \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ CADASIL \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Camurati-Engelmann Syndrome Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Developmental ∟ Osteochondrodysplasias ∟ Camurati-Engelmann Syndrome 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) X
historyNote*:	2007(1975) X
publicMeSHNote*:	2007; see OSTEOCHONDRODYSPLASIAS 1985-1990, see BONE DISEASES, DEVELOPMENTAL 1975-1984 X
Scope note:	An autosomal dominant form of dysplasia that is characterized by progressive thickening of diaphyseal cortex of long bones. Mutations in the gene that encodes TRANSFORMING GROWTH FACTOR BETA1 are one cause of this disorder. X
activeMeSHYear*:	2007X
dateCreated*:	1974-11-11X
dateEstablished*:	1991-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	jmpX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Achondroplasia \| Acquired Hyperostosis Syndrome \| Chondrodysplasia Punctata \| Cleidocranial Dysplasia \| Ellis-Van Creveld Syndrome \| Enchondromatosis \| Fibrous Dysplasia of Bone \| Hyperostosis Frontalis Interna \| Hyperostosis, Cortical, Congenital \| Langer-Giedion Syndrome \| Osteochondroma \| Osteogenesis Imperfecta \| Osteosclerosis \| Short Rib-Polydactyly Syndrome \| Thanatophoric Dysplasia \| Adrenal Hyperplasia, Congenital \| Anemia, Hemolytic, Congenital \| Anemia, Hypoplastic, Congenital \| Ataxia Telangiectasia \| Blood Coagulation Disorders, Inherited \| Brugada Syndrome \| CADASIL \| Cardiomyopathy, Hypertrophic, Familial \| Cherubism \| Chromosome Disorders \| Cystic Fibrosis \| Dwarfism \| Eye Diseases, Hereditary \| Familial Mediterranean Fever \| Genetic Diseases, X-Linked \| Genetic Diseases, Y-Linked \| Hajdu-Cheney Syndrome \| Hemoglobinopathies \| Heredodegenerative Disorders, Nervous System \| Hyperthyroxinemia, Familial Dysalbuminemic \| Jervell-Lange Nielsen Syndrome \| Kallmann Syndrome \| Kartagener Syndrome \| Marfan Syndrome \| Metabolism, Inborn Errors \| Muscular Dystrophies \| Myasthenic Syndromes, Congenital \| Nail-Patella Syndrome \| Neoplastic Syndromes, Hereditary \| Pain Insensitivity, Congenital \| Romano-Ward Syndrome \| Skin Diseases, Genetic \| Werner Syndrome X
URI:	X
Labels and equivalent concepts:	Progressiivinen diafyseaalinen dysplasia (fi) Progressiivinen diafyysidysplasia (fi, replaced) Engelmannin tauti (fi, replaced) Camurati-Engelmannin syndrooma (fi, replaced) Camurati-Engelmannin oireyhtymä (fi, replaced) Diaphyseal Dysplasia, Progressive (en, replaced) Engelmann Disease (en, replaced) Engelmann's Disease (en, replaced) Camurati-Engelmann Disease (en, replaced) Dysplasia diaphysialis progressiva (la-FI, replaced) Morbus Engelmann (la-FI, replaced) Syndroma Camurati-Engelmann (la-FI, replaced) X
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