Concept information
Preferred term
Elliptocytosis, Hereditary
Type
-
Topical Descriptor
Broader concept
Entry terms
- Hereditary Ovalocytoses
- Hereditary Ovalocytosis
- Ovalocytoses, Hereditary
- Ovalocytosis, Hereditary
Note
- a congen hemolytic anemia; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
Scope note
- An intrinsic defect of erythrocytes inherited as an autosomal dominant trait. The erythrocytes assume an oval or elliptical shape.
History note
- 65(64)
In other languages
-
Finnish
-
elliptocytos kongenital
-
elliptocytosis
-
elliptocytosis congenita
-
elliptocytosis hereditaria
-
elliptosytoosi
-
hereditaarinen elliptosytoosi
-
hereditaarinen ovalosytoosi
-
hereditär elliptocytos
-
hereditäärinen elliptosytoosi
-
hereditäärinen ovalosytoosi
-
ovalocytos kongenital hereditär
-
ovalocytosis
-
ovalocytosis congenita
-
ovalocytosis hereditaria
-
perinnöllinen ovalosytoosi
-
periytyvä elliptosytoosi
-
periytyvä ovalosytoosi
-
synnynnäinen elliptosytoosi
-
synnynnäinen ovalosytoosi
-
Swedish
-
Hereditär ovalocytos
-
Ärftlig elliptocytos
URI
http://www.yso.fi/onto/mesh/D004612
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