kongenitální hemolytická anemie [Anemia, Hemolytic, Congenital]
- Termíny
-
anemie hemolytická kongenitální
anémie hemolytická kongenitální
dědičná hemolytická anemie
hemolytická anemie kongenitální
-
Anemia, Hemolytic, Hereditary
Congenital Hemolytic Anemia
Hemolytic Anemia, Congenital
Hemolytic Anemia, Hereditary
Hereditary Hemolytic Anemia
Hemolytická anemie způsobená různými vnitřními poruchami erytrocytů.
Hemolytic anemia due to various intrinsic defects of the erythrocyte.
- DUI
- D000745 MeSH Prohlížeč
- CUI
- M0001129
- Historická pozn.
- 68; was ANEMIA, CONGENITAL HEMOLYTIC 1965-67, was ANEMIA, CONGENITAL HEMOLYTIC see SPHEROCYTOSIS, HEREDITARY 1963-64
- Online pozn.
- use ANEMIA, HEMOLYTIC, CONGENITAL to search ANEMIA, CONGENITAL HEMOLYTIC 1966-67
- Veřejná pozn.
- 68; was ANEMIA, CONGENITAL HEMOLYTIC 1965-67, was ANEMIA, CONGENITAL HEMOLYTIC see SPHEROCYTOSIS, HEREDITARY 1963-64; ANEMIA, HEMOLYTIC, CONGENITAL NONSPHEROCYTIC was heading 1968-81, was ANEMIA, CONGENITAL NON-SPHEROCYTIC HEMOLYTIC 1965-67
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Heinz Body Anemias Disease MeSH Prohlížeč
Hemolytic Anemia, Congenital, with Emphysema and Cutis Laxa Disease MeSH Prohlížeč
Hemolytic Anemia, Lethal Congenital Nonspherocytic, with Genital and Other Abnormalities Disease MeSH Prohlížeč
Red cell phospholipid defect with hemolysis Disease MeSH Prohlížeč
Rh-Null Disease, Amorph Type Disease MeSH Prohlížeč
Stomatocytosis I Disease MeSH Prohlížeč
Stomatocytosis II Disease MeSH Prohlížeč
Transient erythroblastopenia of childhood Disease MeSH Prohlížeč
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to Disease MeSH Prohlížeč
Xerocytosis, hereditary Disease MeSH Prohlížeč