Simplifying Science
™
Loading Search Box, Please Wait ...
Descipher Site Search
Try our new low-cost Blog Generator (click logo). Free trial: 30 blog posts.
Site Browser History
☚
Blood Disorders D
☚
5 aminosalicylic acid
Site Browser History
☚
Blood Disorders D
☚
5 aminosalicylic acid
DESCIPHER HEALTH ➤
Diseases
Disease by Name
Disease by Category
Lab Tests
Tests by Name
Tests by Source
Drugs
Drugs by Generic Name
Drugs by Class
Clinical Findings
Symptoms
Signs
Home
Health
Diseases & Conditions
Permutation Index
Categories
Blood Disorders
Current:
Blood Disorders D
S
T
E
M
Disease and Condition Index for Blood Disorders D
Name Permutations by Letter
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
SORT ORDER:
Name
Category
D Punjab disease, hemoglobin
DBA
deafness, thiamine-responsive megaloblastic anemia with diabetes mellitus and sensorineural
decreased-oxygen-affinity hemoglobinopathy
defect, coagulation
defect, enterocyte intrinsic factor receptor
defect, unspecified, qualitative platelet
defibrination syndrome
deficiency anemia, amino acid
deficiency anemia, folate
deficiency anemia, folic acid
deficiency anemia, iron-refractory iron
deficiency anemia, nutritional iron
deficiency anemia, unspecified, iron
deficiency anemia, unspecified, protein
deficiency anemia, vitamin B12
deficiency anemia, vitamin B6
deficiency hemolytic anemia, P5N
deficiency hemolytic anemia, UMPH1
deficiency hemolytic anemia, uridine 5'-monophosphate nucleotidase
deficiency sideroblastic anemia, copper
deficiency sideroblastic anemia, pyridoxine
deficiency syndrome, dense-granule
deficiency syndrome, Rh
deficiency, acquired coagulation factor
deficiency, acquired protein C
deficiency, acquired protein S
deficiency, AHG
deficiency, antihemophilic globulin
deficiency, antithrombin
deficiency, antithrombin III
deficiency, AT
deficiency, autoimmune protein C
deficiency, autosomal dominant PROC
deficiency, autosomal dominant protein C
deficiency, autosomal recessive PROC
deficiency, autosomal recessive protein C
deficiency, congenital factor I
deficiency, congenital protein C
deficiency, congenital protein S
deficiency, COX1
deficiency, cyclooxygenase 1
deficiency, CYP5A1
deficiency, DHFR
deficiency, diaphorase
deficiency, dihydrofolate reductase
deficiency, erythrocyte CD59
deficiency, erythrocyte hexokinase
deficiency, erythrocyte phosphofructokinase
deficiency, erythrocyte pyruvate kinase
deficiency, extrinsic factor
deficiency, factor II
deficiency, factor IX
deficiency, factor IX functional
deficiency, factor V
deficiency, factor VII
deficiency, factor VIII
deficiency, factor VIII functional
deficiency, factor X
deficiency, factor XII
deficiency, factor XIII
deficiency, fibrin-stabilizing factor
deficiency, formiminotransferase
deficiency, FSF
deficiency, G-6-PD
deficiency, G6PD
deficiency, glucose phosphate isomerase
deficiency, glucose-6-phosphate dehydrogenase
deficiency, glutamate formiminotransferase
deficiency, glutathione synthetase
deficiency, glycoprotein complex IIb-IIIa
deficiency, GP IIb-IIIa complex
deficiency, Hageman factor
deficiency, hereditary MPO
deficiency, hereditary myeloperoxidase
deficiency, intrinsic factor
deficiency, labile factor
deficiency, liver-type pyruvate kinase
deficiency, methemoglobin reductase
deficiency, methylene tetrahydrofolate reductase
deficiency, MPO
deficiency, MTHFR
deficiency, myeloperoxidase
deficiency, NADH-cytochrome b5 reductase
deficiency, NADH-dependent methemoglobin reductase
deficiency, nonspherocytic hemolytic anemia due to G6PD
deficiency, P5N
deficiency, PFK
deficiency, PK
deficiency, PK1
deficiency, plasma thromboplastin antecedent
deficiency, plasma thromboplastin component
deficiency, platelet alpha-granule
deficiency, platelet cyclooxygenase
deficiency, platelet fibrinogen receptor
deficiency, platelet glycoprotein Ib
deficiency, platelet glycoprotein IIb-IIIa
deficiency, platelet thomboxane A synthase
deficiency, prostaglandin-endoperoxidase synthase
deficiency, prothrombin
deficiency, PTA
deficiency, PTC
deficiency, PTGS
deficiency, pyruvate kinase 1
deficiency, red-cell-type pyruvate kinase
deficiency, stable factor
deficiency, Stuart factor
deficiency, Stuart-Prower factor
deficiency, thromboxane A synthase 1
deficiency, thromboxane synthetase
deficiency, TPI
deficiency, triosephosphate isomerase
deficiency, Type I plasminogen
deficiency, Type II plasminogen
deficiency, UMPH1
deficiency, unspecified, plasminogen
deficiency, von Willebrand factor
deficiency, von Willebrand factor receptor
dehydrated hereditary stomatocytosis
dehydrogenase deficiency, glucose-6-phosphate
deletion syndrome, chromosome 1q21.1
delta storage pool disease
dense-granule deficiency syndrome
depression, bone marrow
dermatopathic lymphadenitis
desiccytosis, hereditary
destruction, posttransfusion platelet
destruction, posttransplantation platelet
DHFR deficiency
DHS
diabetes mellitus and sensorineural deafness, thiamine-responsive megaloblastic anemia with
Diamond-Blackfan anemia
diaphorase deficiency
diathesis and pigmented reticuloendothelial cells, albinism with hemorrhagic
DIC
DIC, acute
DIC, chronic
dihydrofolate reductase deficiency
dilutional thrombocytopenia
displaced spleen
disseminated intravascular coagulation
disseminated intravascular coagulation, acute
disseminated intravascular coagulation, chronic
dominant Bernard-Soulier syndrome, autosomal
dominant congenital neutropenia, autosomal
dominant hereditary protein C thrombophilia, autosomal
dominant hereditary protein S thrombophilia, autosomal
dominant HIES, autosomal
dominant hyper-IgE recurrent infection syndrome, autosomal
dominant hyper-IgE syndrome, autosomal
dominant hyperimmunoglobulin E syndrome, autosomal
dominant PROC deficiency, autosomal
dominant protein C deficiency, autosomal
dominant sideroblastic anemia, autosomal
Donath-Landsteiner syndrome
drifting spleen
drug-induced aplastic anemia
drug-induced hemolytic anemia
drug-induced immune hemolytic anemia
drug-induced neutropenia
drug-induced red cell aplasia
drug-induced sideroblastic anemia
drug-induced thrombocytopenia
due to G6PD deficiency, nonspherocytic hemolytic anemia
dyscrasia, blood
dyserythropoietic anemia Type I, congenital
dyserythropoietic anemia Type II, congenital
dyserythropoietic anemia Type III, congenital
dysfibrinogenemia, congenital
dysfunction, pancreatic insufficiency and bone marrow
dysgenesis, periodic platelet
dysgenesis, tidal platelet
dysphagia, sideropenic
dysplasminogenemia
dyssplenism
dysthrombocytopenia, periodic