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282 Hereditary hemolytic anemias
282.0 Hereditary spherocytosis
Acholuric (familial) jaundice
Congenital spherocytosis
Minkowski-Chauffard syndrome
282.1 Hereditary elliptocytosis
Elliptocytosis (congenital)
Ovalocytosis (congenital) (hereditary)
282.2 Anemias due to disorders of glutathione metabolism
Anemia:
enzyme-deficiency, drug induced
erythrocytic glutathione deficiency
glucose-6-phosphate dehydrogenase [G-6-PD] deficiency
glutathione-reductase deficiency
hemolytic nonspherocytic (hereditary), type I
Favism
282.3 Other hemolytic anemias due to enzyme deficiency
Anemia:
hemolytic nonspherocytic (hereditary), type II
hexokinase deficiency
pyruvate-kinase [PK] deficiency
triose phosphate isomerase deficiency
282.4 Thalassemias
Cooley's anemia
Mediterranean anemia (with other hemoglobinopathy)
Sickle-cell thalassemia
Thalassemia (alpha) (beta) (intermedia) (major) (minor) (mixed) (trait)
(with other hemoglobinopathy)
282.5 Sickle-cell trait
Hb-AS genotype
Hemoglobin S [Hb-S] trait
Heterozygous:
hemoglobin S
Hb-S
Excludes: with other hemoglobinopathy (282.6-)
with thalassemia (282.4)
282.6 Sickle-cell anemia
Hb-S disease Sickle-cell/Hb-C disease
Hb-S/Hb-C disease Sickle-cell/Hb-D disease
Hb-S/Hb-D disease Sickle-cell/Hb-E disease
Hb-S/Hb-E disease
Excludes: sickle-cell thalassemia (282.4)
282.7 Other hemoglobinopathies
Abnormal hemoglobin NOS Hemoglobinopathy NOS
Congenital Heinz-body anemia Hereditary persistence of fetal
Disease: hemoglobin [HPFH]
Hb-C Unstable hemoglobin hemolytic disease
Hb-D
Hb-E
Excludes: familial polycythemia (289.6)
Hb-M disease (289.7)
high-oxygen-affinity hemoglobin (289.0)
282.8 Other
Stomatocytosis
282.9 Unspecified
Hereditary hemolytic anemia NOS
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