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

Anemia, Hemolytic, Congenital Nonspherocytic

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Anemia, Hemolytic, Congenital ∟ Anemia, Hemolytic, Congenital Nonspherocytic 7 coordinate concepts ∟ Anemia, Dyserythropoietic, Congenital \| ∟ Anemia, Sickle Cell \| ∟ Elliptocytosis, Hereditary \| ∟ Glucosephosphate Dehydrogenase Deficiency \| ∟ Hemoglobin C Disease \| ∟ Spherocytosis, Hereditary \| ∟ Thalassemia Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Anemia ∟ Anemia, Hemolytic ∟ Anemia, Hemolytic, Congenital ∟ Anemia, Hemolytic, Congenital Nonspherocytic 7 coordinate concepts ∟ Anemia, Dyserythropoietic, Congenital \| ∟ Anemia, Sickle Cell \| ∟ Elliptocytosis, Hereditary \| ∟ Glucosephosphate Dehydrogenase Deficiency \| ∟ Hemoglobin C Disease \| ∟ Spherocytosis, Hereditary \| ∟ Thalassemia X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Anemia, Hemolytic, Congenital ∟ Anemia, Hemolytic, Congenital Nonspherocytic Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Anemia ∟ Anemia, Hemolytic ∟ Anemia, Hemolytic, Congenital ∟ Anemia, Hemolytic, Congenital Nonspherocytic Anemia, Hemolytic, Congenital > 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) X
Annotation:	do not use /congen & do not coord with INFANT, NEWBORN, DISEASES; DF: ANEMIA HEMOL CONGEN NONSPHER X
historyNote*:	91(82)68; was see under ANEMIA, HEMOLYTIC, CONGENITAL 1982-90; was heading 1968-81; was ANEMIA, CONGENITAL NONSPHEROCYTIC HEMOLYTIC 1965-67 X
onlineNote*:	use ANEMIA, HEMOLYTIC, CONGENITAL NONSPHEROCYTIC to search ANEMIA, CONGENITAL NON-SPHEROCYTIC HEMOLYTIC 1966-67 X
publicMeSHNote*:	91,68; was see under ANEMIA, HEMOLYTIC, CONGENITAL 1982-90; was heading 1968-81; was ANEMIA, CONGENITAL NONSPHEROCYTIC HEMOLYTIC 1965-67 X
Scope note:	Any one of a group of congenital hemolytic anemias in which there is no abnormal hemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. In some cases, pyruvate kinase deficiency has been demonstrated; in other cases, glucose-6-phosphate dehydrogenase deficiency has been demonstrated. X
activeMeSHYear*:	2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1968-01-01X
dateRevised*:	2001-07-25X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Anemia, Dyserythropoietic, Congenital \| Anemia, Sickle Cell \| Elliptocytosis, Hereditary \| Glucosephosphate Dehydrogenase Deficiency \| Hemoglobin C Disease \| Spherocytosis, Hereditary \| Thalassemia X
URI:	X
Labels and equivalent concepts:	Synnynnäinen hemolyyttinen ei-sferosytoottinen anemia (fi) Anemia, hemolyyttinen ei-sferosyyttinen, synnynnäinen (fi, replaced) Kongenitaalinen hemolyyttinen ei-sferosytoottinen anemia (fi, replaced) Anemi, hemolytisk, medfödd icke-sfärocytisk (sv) Hemolytic Anemia, Congenital Nonspherocytic (en, replaced) Congenital Nonspherocytic Hemolytic Anemia (en, replaced) Anemia, Hemolytic Congenital, Nonspherocytic (en, replaced) Anemia, Congenital Nonspherocytic Hemolytic (en, replaced) X
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