ONKI3 | Medical Subject Headings

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Anemia, Hemolytic, Congenital ∟ Thalassemia 7 coordinate concepts 2 subordinate concepts ∟ alpha-Thalassemia \| ∟ beta-Thalassemia ∟ Anemia, Dyserythropoietic, Congenital \| ∟ Anemia, Hemolytic, Congenital Nonspherocytic \| ∟ Anemia, Sickle Cell \| ∟ Elliptocytosis, Hereditary \| ∟ Glucosephosphate Dehydrogenase Deficiency \| ∟ Hemoglobin C Disease \| ∟ Spherocytosis, Hereditary Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Hemoglobinopathies ∟ Thalassemia 7 coordinate concepts 2 subordinate concepts ∟ alpha-Thalassemia \| ∟ beta-Thalassemia ∟ Anemia, Dyserythropoietic, Congenital \| ∟ Anemia, Hemolytic, Congenital Nonspherocytic \| ∟ Anemia, Sickle Cell \| ∟ Elliptocytosis, Hereditary \| ∟ Glucosephosphate Dehydrogenase Deficiency \| ∟ Hemoglobin C Disease \| ∟ Spherocytosis, Hereditary Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Anemia ∟ Anemia, Hemolytic ∟ Anemia, Hemolytic, Congenital ∟ Thalassemia 7 coordinate concepts 2 subordinate concepts ∟ alpha-Thalassemia \| ∟ beta-Thalassemia ∟ Anemia, Dyserythropoietic, Congenital \| ∟ Anemia, Hemolytic, Congenital Nonspherocytic \| ∟ Anemia, Sickle Cell \| ∟ Elliptocytosis, Hereditary \| ∟ Glucosephosphate Dehydrogenase Deficiency \| ∟ Hemoglobin C Disease \| ∟ Spherocytosis, Hereditary Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Hemoglobinopathies ∟ Thalassemia 7 coordinate concepts 2 subordinate concepts ∟ alpha-Thalassemia \| ∟ beta-Thalassemia ∟ Anemia, Dyserythropoietic, Congenital \| ∟ Anemia, Hemolytic, Congenital Nonspherocytic \| ∟ Anemia, Sickle Cell \| ∟ Elliptocytosis, Hereditary \| ∟ Glucosephosphate Dehydrogenase Deficiency \| ∟ Hemoglobin C Disease \| ∟ Spherocytosis, Hereditary X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Anemia, Hemolytic, Congenital ∟ Thalassemia Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Hemoglobinopathies ∟ Thalassemia Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Anemia ∟ Anemia, Hemolytic ∟ Anemia, Hemolytic, Congenital ∟ Thalassemia Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Hemoglobinopathies ∟ Thalassemia Anemia, Hemolytic, Congenital > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Hemoglobinopathies > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Anemia, Hemolytic, Congenital > Anemia, Hemolytic > Anemia > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) Hemoglobinopathies > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	alpha-Thalassemia \| beta-Thalassemia X
Annotation:	a congen hemolytic anemia; GEN or unspecified: prefer specifics; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES X
historyNote*:	65; was ANEMIA, ERYTHROBLASTIC 1963-64; ANEMIA, TARGET-CELL was see THALASSEMIA 1965-92 X
onlineNote*:	use THALASSEMIA to search ANEMIA, TARGET-CELL 1966-92 X
publicMeSHNote*:	65; was ANEMIA, ERYTHROBLASTIC 1963-64; ANEMIA, TARGET-CELL was see THALASSEMIA 1965-92 X
Scope note:	A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia. 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:	Anemia, Dyserythropoietic, Congenital \| Anemia, Hemolytic, Congenital Nonspherocytic \| Anemia, Sickle Cell \| Elliptocytosis, Hereditary \| Glucosephosphate Dehydrogenase Deficiency \| Hemoglobin C Disease \| Spherocytosis, Hereditary X
URI:	X
Labels and equivalent concepts:	Talassemia (fi) Välimerenanemia (fi, replaced) Anemia, Välimeren (fi, replaced) Anemia, talassemia- (fi, replaced) Talassemi (sv) Thalassaemia (la-FI, replaced) Anaemia mediterranea (la-FI, replaced) X
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