Condition

Hereditary elliptocytosis

Diseases of the Blood and Immune Mechanism

Hereditary elliptocytosis, also known as ovalocytosis, is an inherited blood disorder in which an unusually large number of a person's red blood cells are elliptical rather than the normal biconcave disc shape. The distinctively shaped cells are sometimes called elliptocytes or ovalocytes. The disorder is one of many defects of the red cell membrane. In its severe forms it predisposes a person to haemolytic anaemia, in which red cells are destroyed faster than they are replaced. The Wikipedia lead adds a comparative note: although the finding is pathological in humans, elliptocytosis is normal in camelids, the family that includes camels and llamas. This entry records the source and is not medical advice.

Facts
Classification
ICD-10 Chapter
III: Diseases of the Blood and Blood-Forming Organs and Certain Disorders Involving the Immune Mechanism 1
Communicable or Non-communicable
Non-Communicable 2
Transmission Route
Non-Transmissible 3
Causative Agent
Causative Agent (category)
Genetic / Hereditary 3
Prevalence Band
Rare (Under 1 in 2000) 4
Sources
1. World Health Organization: ICD-10 Version:2019 - D58.1
World Health OrganizationICD-10 2019 category D58.1
Quote, ICD-10 2019 category D58.1
D58.1 Hereditary elliptocytosis
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2. National Cancer Institute (NCI Thesaurus): Hereditary elliptocytosis - NCI Thesaurus concept C35882
National Cancer Institute (NCI Thesaurus)Definition
Quote, Definition
An inherited blood disorder in which a large number of red blood cells have an elliptical morphology.
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3. Hereditary elliptocytosis (Wikipedia)
  • Lead paragraph
    is an inherited blood disorder
  • Lead
    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.
View the Source
4. Orphadata (Orphanet): Orphadata: Epidemiology of rare diseases (en_product9_prev)
Orphadata (Orphanet)ORPHA:288
Quote, ORPHA:288
Point prevalence Class only 1-5 / 10 000
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