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

Elliptocytosis, Hereditary

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Anemia, Hemolytic, Congenital ∟ Elliptocytosis, Hereditary 7 coordinate concepts ∟ Anemia, Dyserythropoietic, Congenital \| ∟ Anemia, Hemolytic, Congenital Nonspherocytic \| ∟ Anemia, Sickle Cell \| ∟ 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 ∟ Elliptocytosis, Hereditary 7 coordinate concepts ∟ Anemia, Dyserythropoietic, Congenital \| ∟ Anemia, Hemolytic, Congenital Nonspherocytic \| ∟ Anemia, Sickle Cell \| ∟ 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 ∟ Elliptocytosis, Hereditary Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Anemia ∟ Anemia, Hemolytic ∟ Anemia, Hemolytic, Congenital ∟ Elliptocytosis, Hereditary 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:	a congen hemolytic anemia; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES X
historyNote*:	65(64) X
publicMeSHNote*:	65 X
Scope note:	An intrinsic defect of erythrocytes inherited as an autosomal dominant trait. The erythrocytes assume an oval or elliptical shape. 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
Related term:	Anemia, Sideroblastic X
Type:	Concept X
Coordinate terms:	Anemia, Dyserythropoietic, Congenital \| Anemia, Hemolytic, Congenital Nonspherocytic \| Anemia, Sickle Cell \| Glucosephosphate Dehydrogenase Deficiency \| Hemoglobin C Disease \| Spherocytosis, Hereditary \| Thalassemia X
URI:	X
Labels and equivalent concepts:	Perinnöllinen elliptosytoosi (fi) Synnynnäinen ovalosytoosi (fi, replaced) Synnynnäinen elliptosytoosi (fi, replaced) Periytyvä ovalosytoosi (fi, replaced) Hereditaarinen ovalosytoosi (fi, replaced) Hereditaarinen elliptosytoosi (fi, replaced) Ovalosyytit (fi, replaced) Ovalosyytti (fi, replaced) Periytyvä elliptosytoosi (fi, replaced) Perinnöllinen ovalosytoosi (fi, replaced) Elliptocytos, ärftlig (sv) Ovalocytosis, Hereditary (en, replaced) Elliptocytosis congenita (la-FI, replaced) Elliptocytosis (la-FI, replaced) Elliptocytosis hereditaria (la-FI, replaced) Ovalocytosis (la-FI, replaced) Ovalocytosis hereditaria (la-FI, replaced) Ovalocytosis congenita (la-FI, replaced) X
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