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Blood Disorders F
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Blood Disorders F
DESCIPHER HEALTH ➤
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Blood Disorders F
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Disease and Condition Index for Blood Disorders F
Name Permutations by Letter
A
B
C
D
E
F
G
H
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K
L
M
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SORT ORDER:
Name
Category
factor deficiency, acquired coagulation
factor deficiency, extrinsic
factor deficiency, fibrin-stabilizing
factor deficiency, Hageman
factor deficiency, intrinsic
factor deficiency, labile
factor deficiency, stable
factor deficiency, Stuart
factor deficiency, Stuart-Prower
factor deficiency, von Willebrand
factor I deficiency, congenital
factor II deficiency
factor IX deficiency
factor IX disorder, congenital
factor IX functional deficiency
factor receptor defect, enterocyte intrinsic
factor receptor deficiency, von Willebrand
factor V deficiency
factor V Leiden thrombophilia
factor VII deficiency
factor VIII deficiency
factor VIII disorder, congenital
factor VIII functional deficiency
factor X deficiency
factor XI disorder, congenital
factor XII deficiency
factor XIII deficiency
familial eosinophilia
familial erythrophagocytic lymphohistiocytosis
familial hemophagocytic lymphohistiocytosis
familial hemophagocytic lymphohistiocytosis 1
familial hemophagocytic lymphohistiocytosis 2
familial hemophagocytic lymphohistiocytosis 3
familial hemophagocytic lymphohistiocytosis 4
familial hemophagocytic lymphohistiocytosis 5
familial hemophagocytic reticulosis
familial hemophilia
familial histiocytic reticulosis
familial leukopenia, benign
familial neutropenia, chronic
familial pancytopenia
familial spherocytosis
Fanconi anemia
Fanconi pancytopenia syndrome
Fanconi panmyelopathy
Fanconi refractory anemia
favism
Fechtner syndrome
FEL
FES
fetal hemoglobin, unspecified, hereditary persistence of
fetalis with hemoglobin Bart's, hydrops
FHL
FHL1
FHL2
FHL3
FHL4
FHL5
FHLH
fibrin-stabilizing factor deficiency
fibrinogen receptor deficiency, platelet
fibrinolysis, pathologic
fibrinolysis, primary
fibrocongestive splenomegaly
fibrosis, hepatolienal
FIGLU-uria
Fisher-Evans syndrome
floating spleen
folate deficiency anemia
folate malabsorption, congenital
folate malabsorption, hereditary
folic acid deficiency anemia
food-cobalamin malabsorption
formiminoglutamic aciduria
formiminotransferase deficiency
formiminotransferase deficiency, glutamate
FSF deficiency
FTNS
functional asplenia
functional deficiency, factor IX
functional deficiency, factor VIII
functional disorder, neutrophil