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Blood Disorders P
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Blood Disorders P
DESCIPHER HEALTH ➤
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Blood Disorders P
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Disease and Condition Index for Blood Disorders P
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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SORT ORDER:
Name
Category
P5N deficiency
P5N deficiency hemolytic anemia
pancreas, congenital lipomatosis of
pancreatic insufficiency and bone marrow dysfunction
pancytopenia
pancytopenia syndrome, Fanconi
pancytopenia, familial
panmyelopathy, Fanconi
parahemophilia
parahemophilia, Owren
Paris-Trousseau-type thrombocytopenia
paroxysmal cold hemoglobinuria
paroxysmal nocturnal hemoglobinuria
Paterson-Brown Kelly syndrome
Paterson-Kelly syndrome
pathologic fibrinolysis
PCH
Pelger-Huet anomaly
peliosis rheumatica
pelvic spleen
periodic dysthrombocytopenia
periodic neutropenia
periodic platelet dysgenesis
periodic thrombocytopenia
pernicious anemia
pernicious anemia, acquired
pernicious anemia, congenital
pernicious anemia, juvenile
persistence of fetal hemoglobin, unspecified, hereditary
PFK deficiency
phosphate isomerase deficiency, glucose
phosphofructokinase deficiency, erythrocyte
pigmented reticuloendothelial cells, albinism with hemorrhagic diathesis and
PK deficiency
PK1 deficiency
plasma thromboplastin antecedent deficiency
plasma thromboplastin component deficiency
plasmacytopenia
plasmacytosis
plasminogen deficiency
plasminogen deficiency, Type I
plasminogen deficiency, Type II
platelet alloimmunization
platelet alpha-granule deficiency
platelet cyclooxygenase deficiency
platelet defect, unspecified, qualitative
platelet destruction, posttransfusion
platelet destruction, posttransplantation
platelet dysgenesis, periodic
platelet dysgenesis, tidal
platelet fibrinogen receptor deficiency
platelet glycoprotein Ib deficiency
platelet glycoprotein IIb-IIIa deficiency
platelet syndrome, Sebastian
platelet thomboxane A synthase deficiency
platelet-type bleeding disorder 1
platelet-type bleeding disorder 12
platelet-type bleeding disorder 12,
platelet-type bleeding disorder 3
platelet-type bleeding disorder 6
platelet-type von Willebrand disease
Plummer-Vinson syndrome
PNH
polycythemia, relative
polycythemia, secondary
polycythemia, stress
pool disease, delta storage
positive hemolytic anemia, Coomb's
posthemorrhagic anemia, acute
posttranfusion thrombocytopenia
posttransfusion platelet destruction
posttransfusion purpura
posttransplantation platelet destruction
potassium-sodium erythrocyte disorder
PRCA
PRCA, acquired
PRCA, hereditary
primary aplastic anemia
primary fibrinolysis
primary hypercoagulable state
primary immune thrombocytopenic purpura
primary thrombocytopenia
PROC deficiency, autosomal dominant
PROC deficiency, autosomal recessive
prostaglandin-endoperoxidase synthase deficiency
protein C deficiency, acquired
protein C deficiency, autoimmune
protein C deficiency, autosomal dominant
protein C deficiency, autosomal recessive
protein C deficiency, congenital
protein C thrombophilia, autosomal dominant hereditary
protein C thrombophilia, autosomal recessive hereditary
protein deficiency anemia
protein S deficiency, acquired
protein S deficiency, congenital
protein S thrombophilia, autosomal dominant hereditary
protein S thrombophilia, autosomal recessive hereditary
prothrombin deficiency
pryoglutamic aciduria
pseudo-von Willebrand disease
pseudotumor, inflammatory lymph node
PTA deficiency
PTC deficiency
PTGS deficiency
ptosis, splenic
Punjab disease, hemoglobin D
pure red cell anemia
pure red cell anemia, hereditary
pure red cell aplasia
pure red cell aplasia, acquired
pure red cell aplasia, congenital
pure red cell aplasia, hereditary
purpura, allergic
purpura, anaphylactoid
purpura, autoimmune thrombocytopenic
purpura, Henoch-Schoenlein
purpura, Henoch-Schonlein
purpura, idiopathic thrombocytopenic
purpura, nonthrombocytopenic idiopathic
purpura, posttransfusion
purpura, primary immune thrombocytopenic
purpura, rheumatic
purpura, Schoenlein-Henoch
purpura, Schonlein-Henoch
PVS
pyridoxine deficiency sideroblastic anemia
pyrimidine 5'-nucleotidase hemolytic anemia
pyropoikilocytosis, hereditary
pyruvate kinase 1 deficiency
pyruvate kinase deficiency, erythrocyte
pyruvate kinase deficiency, liver-type
pyruvate kinase deficiency, red-cell-type