Anaemia (due to):enzyme deficiencies, except G6PD, related to the hexose monophosphate [HMP] shunt pathway | haemolytic nonspherocytic (hereditary), type I

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

Anémie (due à):déficit enzymatique, excepté G6PD, de la voie de l'hexose monophosphate [HMP] | hémolytique non sphérocytaire (héréditaire), type I

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]

Anaemia:haemolytic nonspherocytic (hereditary), type II | hexokinase deficiency | pyruvate kinase [PK] deficiency | triose-phosphate isomerase deficiency

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

Anémie (due à):déficit en:hexokinase | pyruvate kinase [PK] | triose-phosphate isomérase | hémolytique non sphérocytaire (héréditaire), type II

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]

hereditary non spherocytic hemolytic anemia

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

anémie héréditaire hémolytique et asphérocytaire

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http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

A rare hereditary red cell membrane defect characterized by the presence of oval-shaped erythrocytes. Most patients are asymptomatic or occasionally have mild symptoms such as pallor, jaundice, anemia and gallstones. The disease is common in Southeas

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

ovalocytose de l'Asie du Sud-Est

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

D'autres ont cherché : cooley's anemia cooley's syndrome cooley's-disease cooley-lee syndrome dameshek's syndrome heinz hereditary bodies anemia mediterranean anemia mediterranean disease chronic familial erythremia congenital non-spherocytic anaemia congenital nonspherocytic anemia deficiency erythroblastic anemia haemolytic nonspherocytic type hereditary leptocytosis hereditary non spherocytic hemolytic anemia hereditary nonspherocytic anemia hexokinase deficiency marcocytic hereditary hemolytic anemia primary erythroblastic anemia pyruvate kinase shunt pathway target cell anemia target-oval cell syndrome thalassaemia major thalassemia major thalassemic syndrome triose-phosphate isomerase deficiency Hereditary nonspherocytic anemia

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'Hereditary nonspherocytic anemia' ->

Date index: 2021-09-11