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About: Hereditary elliptocytosis     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : umbel-rc:AilmentCondition, within Data Space : dbpedia.demo.openlinksw.com associated with source document(s)

Type: ThingDiseaseyago:WikicatAnemiasyago:WikicatAutosomalDominantDisordersyago:Abstraction100002137yago:Anemia114195315yago:Attribute100024264yago:AutosomalDominantDisease114162025yago:BloodDisease114189204yago:BloodDyscrasia114053850yago:Condition113920835yago:Disease114070360yago:Dyscrasia114053717yago:GeneticDisease114151139yago:HemolyticAnemia114165240yago:IllHealth114052046yago:Illness114061805yago:PathologicalState114051917yago:PhysicalCondition114034177yago:WikicatHereditaryHemolyticAnemiasdiseaseyago:State100024720umbel-rc:AilmentCondition New Facet based on Instances of this Class

Hereditary elliptocytosis, also known as ovalocytosis, is an inherited blood disorder in which an abnormally large number of the person's red blood cells are elliptical rather than the typical biconcave disc shape. Such morphologically distinctive erythrocytes are sometimes referred to as elliptocytes or ovalocytes. It is one of many red-cell membrane defects. In its severe forms, this disorder predisposes to haemolytic anaemia. Although pathological in humans, elliptocytosis is normal in camelids.