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Blood Disorders C
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Blood Disorders C
DESCIPHER HEALTH ➤
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Blood Disorders C
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Disease and Condition Index for Blood Disorders C
Name Permutations by Letter
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
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X
SORT ORDER:
Name
Category
capillary toxicosis, hemorrhagic
carrier, alpha-thalassemia
carrier, beta-thalassemia
caused hemoglobinuria, unspecified, externally
CC, Hb
CC, hemoglobin
CC, Hgb
CD4 lymphocytopenia, idiopathic
CD59 deficiency, erythrocyte
CDA I
CDA II
CDA III
CDAN1
CDAN2
CDAN3
cell anemia, hereditary pure red
cell anemia, spur
cell anemia, unspecified, pure red
cell aplasia, acquired pure red
cell aplasia, congenital pure red
cell aplasia, drug-induced red
cell aplasia, hereditary pure red
cell aplasia, unspecified, pure red
cell disorder, white blood
cell hemolytic anemia, spur
cells, albinism with hemorrhagic diathesis and pigmented reticuloendothelial
CGD
Chediak-Higashi syndrome
Chediak-Steinbrinck syndrome
Chediak-Steinbrinck-Higashi syndrome
childhood, transient erythroblastopenia of
Christmas disease
chromosome 1q21.1 deletion syndrome
chronic blood-loss anemia
chronic congenital aregenerative anemia
chronic congestive splenomegaly
chronic DIC
chronic disease, anemia of
chronic disseminated intravascular coagulation
chronic familial neutropenia
chronic granulomatous disease
chronic idiopathic neutropenia, nonimmune
chronic idiopathic neutrophilia
chronic illness, anemia of
chronic intravascular hemolysis
chronic liver disease, anemia of
chronic lymphadenitis
chronic-disease anemia
chronic-renal-failure anemia
CHS
circulating-anticoagulant hemorrhagic disorder
cirrhotic splenomegaly
classical hemophilia
clotting disorder
coagulation defect
coagulation disorder
coagulation factor deficiency, acquired
coagulation, acute disseminated intravascular
coagulation, chronic disseminated intravascular
coagulation, disseminated intravascular
coagulopathy
coagulopathy, consumption
cobalamin malabsorption, enterocyte
cold agglutinin disease
cold and warm antibody hemolytic anemia, combined
cold antibody AIHA
cold antibody hemolytic anemia
cold hemoglobinuria, paroxysmal
combined cold and warm antibody hemolytic anemia
compensated hemolysis
compensated hemolytic anemia
complex deficiency, GP IIb-IIIa
complex IIb-IIIa deficiency, glycoprotein
component deficiency, plasma thromboplastin
condition, unspecified, hemorrhagic
congenital afibrinogenemia
congenital aplastic anemia
congenital aregenerative anemia, chronic
congenital dyserythropoietic anemia Type I
congenital dyserythropoietic anemia Type II
congenital dyserythropoietic anemia Type III
congenital dysfibrinogenemia
congenital elliptocytosis
congenital erythroid hypoplastic anemia
congenital factor I deficiency
congenital factor IX disorder
congenital factor VIII disorder
congenital factor XI disorder
congenital folate malabsorption
congenital hypodysfibrinogenemia
congenital hypofibrinogenemia
congenital lipomatosis of pancreas
congenital neutropenia, autosomal dominant
congenital neutropenia, severe
congenital neutropenia, sporadic
congenital ovalocytosis
congenital pernicious anemia
congenital protein C deficiency
congenital protein S deficiency
congenital pure red cell aplasia
congenital sideroblastic anemia, B6-responsive
congenital spherocytic anemia
congenital X-linked sideroblastic anemia
congestive splenomegaly
congestive splenomegaly, chronic
consumption coagulopathy
Cooley's anemia
Cooley's trait
Coomb's negative hemolytic anemia
Coomb's positive hemolytic anemia
copper deficiency sideroblastic anemia
COX1 deficiency
crisis, hemolytic
crisis, sickle-cell
cryopathic hemolytic syndrome
cyclic hematopoiesis
cyclic neutropenia
cyclooxygenase 1 deficiency
cyclooxygenase deficiency, platelet
CYP5A1 deficiency
cytopathic sideroblastic anemia, mitochondrial