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Severe Combined Immunodeficiency

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Infant, Newborn, Diseases ∟ Severe Combined Immunodeficiency 47 coordinate concepts 1 subordinate concept ∟ X-Linked Combined Immunodeficiency Diseases ∟ Ataxia Telangiectasia \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Colorectal Neoplasms, Hereditary Nonpolyposis \| ∟ Fanconi Anemia \| ∟ Li-Fraumeni Syndrome \| ∟ Nijmegen Breakage Syndrome \| ∟ Rothmund-Thomson Syndrome \| ∟ Werner Syndrome \| ∟ Xeroderma Pigmentosum \| ∟ Agammaglobulinemia \| ∟ Common Variable Immunodeficiency \| ∟ Deltaretrovirus Infections \| ∟ DiGeorge Syndrome \| ∟ Dysgammaglobulinemia \| ∟ HIV Infections \| ∟ Leukocyte-Adhesion Deficiency Syndrome \| ∟ Lymphopenia \| ∟ Phagocyte Bactericidal Dysfunction \| ∟ Wiskott-Aldrich Syndrome \| ∟ 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 \| ∟ Hyperostosis, Cortical, Congenital \| ∟ 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 \| ∟ Sclerema Neonatorum \| ∟ Syphilis, Congenital \| ∟ Thanatophoric Dysplasia \| ∟ Toxoplasmosis, Congenital \| ∟ Wolman Disease Medical Subject Headings (MeSH) ∟ Immune System Diseases ∟ Immunologic Deficiency Syndromes ∟ Severe Combined Immunodeficiency 47 coordinate concepts 1 subordinate concept ∟ X-Linked Combined Immunodeficiency Diseases ∟ Ataxia Telangiectasia \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Colorectal Neoplasms, Hereditary Nonpolyposis \| ∟ Fanconi Anemia \| ∟ Li-Fraumeni Syndrome \| ∟ Nijmegen Breakage Syndrome \| ∟ Rothmund-Thomson Syndrome \| ∟ Werner Syndrome \| ∟ Xeroderma Pigmentosum \| ∟ Agammaglobulinemia \| ∟ Common Variable Immunodeficiency \| ∟ Deltaretrovirus Infections \| ∟ DiGeorge Syndrome \| ∟ Dysgammaglobulinemia \| ∟ HIV Infections \| ∟ Leukocyte-Adhesion Deficiency Syndrome \| ∟ Lymphopenia \| ∟ Phagocyte Bactericidal Dysfunction \| ∟ Wiskott-Aldrich Syndrome \| ∟ 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 \| ∟ Hyperostosis, Cortical, Congenital \| ∟ 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 \| ∟ Sclerema Neonatorum \| ∟ Syphilis, Congenital \| ∟ Thanatophoric Dysplasia \| ∟ Toxoplasmosis, Congenital \| ∟ Wolman Disease Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ DNA Repair-Deficiency Disorders ∟ Severe Combined Immunodeficiency 47 coordinate concepts 1 subordinate concept ∟ X-Linked Combined Immunodeficiency Diseases ∟ Ataxia Telangiectasia \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Colorectal Neoplasms, Hereditary Nonpolyposis \| ∟ Fanconi Anemia \| ∟ Li-Fraumeni Syndrome \| ∟ Nijmegen Breakage Syndrome \| ∟ Rothmund-Thomson Syndrome \| ∟ Werner Syndrome \| ∟ Xeroderma Pigmentosum \| ∟ Agammaglobulinemia \| ∟ Common Variable Immunodeficiency \| ∟ Deltaretrovirus Infections \| ∟ DiGeorge Syndrome \| ∟ Dysgammaglobulinemia \| ∟ HIV Infections \| ∟ Leukocyte-Adhesion Deficiency Syndrome \| ∟ Lymphopenia \| ∟ Phagocyte Bactericidal Dysfunction \| ∟ Wiskott-Aldrich Syndrome \| ∟ 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 \| ∟ Hyperostosis, Cortical, Congenital \| ∟ 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 \| ∟ Sclerema Neonatorum \| ∟ Syphilis, Congenital \| ∟ Thanatophoric Dysplasia \| ∟ Toxoplasmosis, Congenital \| ∟ Wolman Disease X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Infant, Newborn, Diseases ∟ Severe Combined Immunodeficiency Medical Subject Headings (MeSH) ∟ Immune System Diseases ∟ Immunologic Deficiency Syndromes ∟ Severe Combined Immunodeficiency Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ DNA Repair-Deficiency Disorders ∟ Severe Combined Immunodeficiency Infant, Newborn, Diseases > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Immunologic Deficiency Syndromes > Immune System Diseases > Medical Subject Headings (MeSH) DNA Repair-Deficiency Disorders > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	X-Linked Combined Immunodeficiency Diseases X
History note:	Immunologic Deficiency Syndromes (1974-1991)X
historyNote*:	92 X
publicMeSHNote*:	92 X
Scope note:	Group of rare congenital disorders characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. It is inherited as an X-linked or autosomal recessive defect. Mutations occurring in many different genes cause human SCID. X
activeMeSHYear*:	2006 \| 2007X
dateCreated*:	1991-01-03X
dateEstablished*:	1992-01-01X
dateRevised*:	2005-06-30X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	AGSX
Type:	Concept X
Coordinate terms:	Ataxia Telangiectasia \| Bloom Syndrome \| Cockayne Syndrome \| Colorectal Neoplasms, Hereditary Nonpolyposis \| Fanconi Anemia \| Li-Fraumeni Syndrome \| Nijmegen Breakage Syndrome \| Rothmund-Thomson Syndrome \| Werner Syndrome \| Xeroderma Pigmentosum \| Agammaglobulinemia \| Common Variable Immunodeficiency \| Deltaretrovirus Infections \| DiGeorge Syndrome \| Dysgammaglobulinemia \| HIV Infections \| Leukocyte-Adhesion Deficiency Syndrome \| Lymphopenia \| Phagocyte Bactericidal Dysfunction \| Wiskott-Aldrich Syndrome \| 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 \| Hyperostosis, Cortical, Congenital \| 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 \| Sclerema Neonatorum \| Syphilis, Congenital \| Thanatophoric Dysplasia \| Toxoplasmosis, Congenital \| Wolman Disease X
URI:	X
Labels and equivalent concepts:	SCID-oireyhtymä (fi) SCID (fi, replaced) SCID-syndroma (fi, replaced) Svår kombinerad immunbrist (sv) SCID (sv, replaced) Svår kombinerad immundefekt (sv, replaced) Severe Combined Immunologic Deficiency (en, replaced) Severe Combined Immunodeficiency Syndrome (en, replaced) Immunodeficiency, Severe Combined (en, replaced) Immunologic Deficiency, Severe Combined (en, replaced) SCID (en, replaced) Immunodeficiency Syndrome, Severe Combined (en, replaced) X
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