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2009 ICD-9-CM

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Disease, diseased - see also Syndrome
AS genotype 282.5
Bart's 282.49
C (Hb-C) 282.7
with other abnormal hemoglobin NEC 282.7
elliptocytosis 282.7
Hb-S (without crisis) 282.63
with
crisis 282.64
vaso-occlusive pain 282.64
sickle-cell (without crisis) 282.63
with
crisis 282.64
vaso-occlusive pain 282.64
thalassemia 282.49
constant spring 282.7
D (Hb-D) 282.7
with other abnormal hemoglobin NEC 282.7
Hb-S (without crisis) 282.68
with crisis 282.69
sickle-cell (without crisis) 282.68
with crisis 282.69
thalassemia 282.49
E (Hb-E) 282.7
with other abnormal hemoglobin NEC 282.7
Hb-S  (without crisis) 282.68
with crisis 282.69
sickle-cell  (without crisis) 282.68
with crisis 282.69
thalassemia 282.49
elliptocytosis 282.7
F (Hb-F) 282.7
G (Hb-G) 282.7
H (Hb-H) 282.49
hereditary persistence, fetal (HPFH) ("Swiss variety") 282.7
high fetal gene 282.7
I thalassemia 282.49
S - see also Disease, sickle-cell, Hb-S
thalassemia (without crisis) 282.41
with
crisis 282.42
vaso-occlusive pain 282.42
spherocytosis 282.7
unstable, hemolytic 282.7
Zurich (Hb-Zurich) 282.7
hemolytic (fetus) (newborn) 773.2
autoimmune (cold type) (warm type) 283.0
due to or with
incompatibility
ABO (blood group) 773.1
 
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