ONKI3 | Medical Subject Headings

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Anemia, Dyserythropoietic, Congenital

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Anemia, Hemolytic, Congenital ∟ Anemia, Dyserythropoietic, Congenital 7 coordinate concepts ∟ Anemia, Hemolytic, Congenital Nonspherocytic \| ∟ 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, Dyserythropoietic, Congenital 7 coordinate concepts ∟ Anemia, Hemolytic, Congenital Nonspherocytic \| ∟ 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, Dyserythropoietic, Congenital Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Anemia ∟ Anemia, Hemolytic ∟ Anemia, Hemolytic, Congenital ∟ Anemia, Dyserythropoietic, Congenital 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
History note:	Anemia (1966-1979) \| Erythropoiesis (1966-1979)X
historyNote*:	91(80); was see under ANEMIA, HEMOLYTIC, CONGENITAL 1980-90 X
publicMeSHNote*:	91; was see under ANEMIA, HEMOLYTIC, CONGENITAL 1980-90 X
Scope note:	A familial disorder characterized by ANEMIA with multinuclear ERYTHROBLASTS, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors (ERYTHROID PROGENITOR CELLS). Type II is the most common of the 3 types; it is often referred to as HEMPAS, based on the Hereditary Erythroblast Multinuclearity with Positive Acidified Serum test. X
activeMeSHYear*:	2006 \| 2007X
dateCreated*:	1979-04-23X
dateEstablished*:	1991-01-01X
dateRevised*:	2005-06-30X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	VDKX
Type:	Concept X
Coordinate terms:	Anemia, Hemolytic, Congenital Nonspherocytic \| Anemia, Sickle Cell \| Elliptocytosis, Hereditary \| Glucosephosphate Dehydrogenase Deficiency \| Hemoglobin C Disease \| Spherocytosis, Hereditary \| Thalassemia X
URI:	X
Labels and equivalent concepts:	Synnynnäinen dyserytropoieettinen anemia (fi) Kongenitaalinen dyserytropoieettinen anemia (fi, replaced) Anemia, dyserytropoieettinen, synnynnäinen (fi, replaced) Synnynnäinen dyshematopoieettinen anemia (fi, replaced) Anemi, dyserytropoietisk, medfödd (sv) Dyserytropoietisk anemi, medfödd (sv, replaced) Hereditary Erythroblast Multinuclearity with Positive Acidified Serum (en, replaced) HEMPAS (en, replaced) Congenital Dyserythropoietic Anemia (en, replaced) Anemia, Congenital Dyserythropoietic, Type II (en, replaced) Congenital Dyserythropoietic Anemia Type II (en, replaced) Congenital Dyserythropoietic Anemia, Type I (en, replaced) Dyserythropoietic Anemia, Congenital (en, replaced) Congenital Dyserythropoietic Anemia, Type III (en, replaced) Anemia, Congenital Dyserythropoietic (en, replaced) Anaemia dyserythropoietica congenita (la-FI, replaced) Anaemia dyshematopoietica congenita (la-FI, replaced) X
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