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

Hyperostosis, Cortical, Congenital

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Infant, Newborn, Diseases ∟ Hyperostosis, Cortical, Congenital 45 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 \| ∟ Langer-Giedion Syndrome \| ∟ Osteochondroma \| ∟ Osteogenesis Imperfecta \| ∟ Osteosclerosis \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Thanatophoric Dysplasia \| ∟ Exostoses \| ∟ Hyperostosis, Diffuse Idiopathic Skeletal \| ∟ Hyperostosis, Sternocostoclavicular \| ∟ Amniotic Band Syndrome \| ∟ Anemia, Neonatal \| ∟ Asphyxia Neonatorum \| ∟ Birth Injuries \| ∟ Cystic Fibrosis \| ∟ Epilepsy, Benign Neonatal \| ∟ Erythroblastosis, Fetal \| ∟ Hemorrhagic Disease of Newborn \| ∟ Hernia, Umbilical \| ∟ Hydrocephalus \| ∟ Hydrophthalmos \| ∟ Hyperbilirubinemia, Neonatal \| ∟ Ichthyosis \| ∟ Infant, Premature, Diseases \| ∟ Meconium Aspiration Syndrome \| ∟ Mobius Syndrome \| ∟ Neonatal Abstinence Syndrome \| ∟ Nystagmus, Congenital \| ∟ Ophthalmia Neonatorum \| ∟ Persistent Fetal Circulation Syndrome \| ∟ Persistent Hyperinsulinemia Hypoglycemia of Infancy \| ∟ Rothmund-Thomson Syndrome \| ∟ Sclerema Neonatorum \| ∟ Severe Combined Immunodeficiency \| ∟ Syphilis, Congenital \| ∟ Toxoplasmosis, Congenital \| ∟ Wolman Disease Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Developmental ∟ Osteochondrodysplasias ∟ Hyperostosis, Cortical, Congenital 45 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 \| ∟ Langer-Giedion Syndrome \| ∟ Osteochondroma \| ∟ Osteogenesis Imperfecta \| ∟ Osteosclerosis \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Thanatophoric Dysplasia \| ∟ Exostoses \| ∟ Hyperostosis, Diffuse Idiopathic Skeletal \| ∟ Hyperostosis, Sternocostoclavicular \| ∟ Amniotic Band Syndrome \| ∟ Anemia, Neonatal \| ∟ Asphyxia Neonatorum \| ∟ Birth Injuries \| ∟ Cystic Fibrosis \| ∟ Epilepsy, Benign Neonatal \| ∟ Erythroblastosis, Fetal \| ∟ Hemorrhagic Disease of Newborn \| ∟ Hernia, Umbilical \| ∟ Hydrocephalus \| ∟ Hydrophthalmos \| ∟ Hyperbilirubinemia, Neonatal \| ∟ Ichthyosis \| ∟ Infant, Premature, Diseases \| ∟ Meconium Aspiration Syndrome \| ∟ Mobius Syndrome \| ∟ Neonatal Abstinence Syndrome \| ∟ Nystagmus, Congenital \| ∟ Ophthalmia Neonatorum \| ∟ Persistent Fetal Circulation Syndrome \| ∟ Persistent Hyperinsulinemia Hypoglycemia of Infancy \| ∟ Rothmund-Thomson Syndrome \| ∟ Sclerema Neonatorum \| ∟ Severe Combined Immunodeficiency \| ∟ Syphilis, Congenital \| ∟ Toxoplasmosis, Congenital \| ∟ Wolman Disease Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Hyperostosis ∟ Hyperostosis, Cortical, Congenital 45 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 \| ∟ Langer-Giedion Syndrome \| ∟ Osteochondroma \| ∟ Osteogenesis Imperfecta \| ∟ Osteosclerosis \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Thanatophoric Dysplasia \| ∟ Exostoses \| ∟ Hyperostosis, Diffuse Idiopathic Skeletal \| ∟ Hyperostosis, Sternocostoclavicular \| ∟ Amniotic Band Syndrome \| ∟ Anemia, Neonatal \| ∟ Asphyxia Neonatorum \| ∟ Birth Injuries \| ∟ Cystic Fibrosis \| ∟ Epilepsy, Benign Neonatal \| ∟ Erythroblastosis, Fetal \| ∟ Hemorrhagic Disease of Newborn \| ∟ Hernia, Umbilical \| ∟ Hydrocephalus \| ∟ Hydrophthalmos \| ∟ Hyperbilirubinemia, Neonatal \| ∟ Ichthyosis \| ∟ Infant, Premature, Diseases \| ∟ Meconium Aspiration Syndrome \| ∟ Mobius Syndrome \| ∟ Neonatal Abstinence Syndrome \| ∟ Nystagmus, Congenital \| ∟ Ophthalmia Neonatorum \| ∟ Persistent Fetal Circulation Syndrome \| ∟ Persistent Hyperinsulinemia Hypoglycemia of Infancy \| ∟ Rothmund-Thomson Syndrome \| ∟ Sclerema Neonatorum \| ∟ Severe Combined Immunodeficiency \| ∟ Syphilis, Congenital \| ∟ Toxoplasmosis, Congenital \| ∟ Wolman Disease X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Infant, Newborn, Diseases ∟ Hyperostosis, Cortical, Congenital Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Developmental ∟ Osteochondrodysplasias ∟ Hyperostosis, Cortical, Congenital Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Hyperostosis ∟ Hyperostosis, Cortical, Congenital Infant, Newborn, Diseases > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Osteochondrodysplasias > Bone Diseases, Developmental > Bone Diseases > Musculoskeletal Diseases > Medical Subject Headings (MeSH) Hyperostosis > Bone Diseases > Musculoskeletal Diseases > Medical Subject Headings (MeSH) X
Annotation:	cortical refers to cortex of bone; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES X
historyNote*:	91; was HYPEROSTOSIS, CORTICAL CONGENITAL 1964-90 X
onlineNote*:	use HYPEROSTOSIS, CORTICAL, CONGENITAL to search HYPEROSTOSIS, CORTICAL CONGENITAL 1966-90 X
publicMeSHNote*:	91; was HYPEROSTOSIS, CORTICAL CONGENITAL 1964-90 X
Scope note:	A disease of young infants characterized by soft tissue swellings over the affected bones, fever, and irritability, and marked by periods of remission and exacerbation. (Dorland, 27th ed) X
activeMeSHYear*:	2000 \| 2001 \| 2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1964-01-01X
dateRevised*:	1999-11-03X
recordAuthorizer*:	sjnX
recordMaintainer*:	kleX
recordOriginator*:	NLMX
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 \| Langer-Giedion Syndrome \| Osteochondroma \| Osteogenesis Imperfecta \| Osteosclerosis \| Short Rib-Polydactyly Syndrome \| Thanatophoric Dysplasia \| Exostoses \| Hyperostosis, Diffuse Idiopathic Skeletal \| Hyperostosis, Sternocostoclavicular \| Amniotic Band Syndrome \| Anemia, Neonatal \| Asphyxia Neonatorum \| Birth Injuries \| Cystic Fibrosis \| Epilepsy, Benign Neonatal \| Erythroblastosis, Fetal \| Hemorrhagic Disease of Newborn \| Hernia, Umbilical \| Hydrocephalus \| Hydrophthalmos \| Hyperbilirubinemia, Neonatal \| Ichthyosis \| Infant, Premature, Diseases \| Meconium Aspiration Syndrome \| Mobius Syndrome \| Neonatal Abstinence Syndrome \| Nystagmus, Congenital \| Ophthalmia Neonatorum \| Persistent Fetal Circulation Syndrome \| Persistent Hyperinsulinemia Hypoglycemia of Infancy \| Rothmund-Thomson Syndrome \| Sclerema Neonatorum \| Severe Combined Immunodeficiency \| Syphilis, Congenital \| Toxoplasmosis, Congenital \| Wolman Disease X
URI:	X
Labels and equivalent concepts:	Synnynnäinen kortikaalinen hyperostoosi (fi) Kongenitaalinen kortikaalinen hyperostoosi (fi, replaced) Hyperostos, kortikal, medfödd (sv) Caffey-De Toni-Silvermanns syndrom (sv, replaced) Infantile Cortical Hyperostosis (en, replaced) Cortical Hyperostosis, Congenital (en, replaced) Congenital Hyperostosis, Cortical (en, replaced) Cortical Congenital Hyperostosis (en, replaced) Caffey-De Toni-Silvermann Syndrome (en, replaced) X
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