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Blood Disorders T
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Blood Disorders T
DESCIPHER HEALTH ➤
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Blood Disorders T
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Disease and Condition Index for Blood Disorders T
Name Permutations by Letter
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SORT ORDER:
Name
Category
TAR syndrome
TCPT
tetrahydrofolate reductase deficiency, methylene
tetraphocomelia-thrombocytopenia syndrome
thalassemia
thalassemia intermedia
thalassemia major
thalassemia minima
thalassemia minor
thalassemia, hemoglobin C - beta
thalassemia, hemoglobin C - beta+
thalassemia, hemoglobin C - beta0
thalassemia, hemoglobin E - beta
thalassemia, hemoglobin S - beta
thalassemia, hemoglobin S - beta+
thalassemia, hemoglobin S - beta0
thalassemia, sickle beta
thalassemia, sickle beta+
thalassemia, sickle beta0
thiamine-responsive anemia syndrome
thiamine-responsive megaloblastic anemia syndrome
thiamine-responsive megaloblastic anemia with diabetes mellitus and sensorineural deafness
thiamine-responsive myelodysplasia
thomboxane A synthase deficiency, platelet
thrombasthenia, Glanzmann
thrombocytopenia
thrombocytopenia absent radius syndrome
thrombocytopenia, dilutional
thrombocytopenia, drug-induced
thrombocytopenia, infection-associated
thrombocytopenia, Paris-Trousseau-type
thrombocytopenia, periodic
thrombocytopenia, posttranfusion
thrombocytopenia, radial aplasia-amegakaryocytic
thrombocytopenia, unspecified, primary
thrombocytopenia, unspecified, secondary
thrombocytopenia-absent radii syndrome
thrombocytopenic purpura, autoimmune
thrombocytopenic purpura, idiopathic
thrombocytopenic purpura, primary immune
thrombophilia, antithrombin II
thrombophilia, autosomal dominant hereditary protein C
thrombophilia, autosomal dominant hereditary protein S
thrombophilia, autosomal recessive hereditary protein C
thrombophilia, autosomal recessive hereditary protein S
thrombophilia, factor V Leiden
thrombophilia, hereditary
thromboplastin antecedent deficiency, plasma
thromboplastin component deficiency, plasma
thromboxane A synthase 1 deficiency
thromboxane synthetase deficiency
tidal platelet dysgenesis
to G6PD deficiency, nonspherocytic hemolytic anemia due
toxic methemoglobinemia
toxic sideroblastic anemia
toxicosis, hemorrhagic capillary
TPI deficiency
trait 1, alpha-thalassemia
trait 2, alpha-thalassemia
trait, beta-thalassemia
trait, Cooley's
trait, Hb-S
trait, hemoglobin C
trait, hemoglobin E
trait, hemoglobin-S
trait, Hgb-S
trait, sickle-cell
transient erythroblastopenia of childhood
triosephosphate isomerase deficiency
TRMA
Type 1 von Willebrand disease
Type 2 von Willebrand disease
Type 2A von Willebrand disease
Type 2B von Willebrand disease
Type 2M von Willebrand disease
Type 2N von Willebrand disease
Type 3 von Willebrand disease
Type A2 Bernard-Soulier syndrome
Type I plasminogen deficiency
Type I von Willebrand disease
Type I, congenital dyserythropoietic anemia
Type II plasminogen deficiency
Type II von Willebrand disease
Type II, congenital dyserythropoietic anemia
Type IIA von Willebrand disease
Type IIB von Willebrand disease
Type III von Willebrand disease
Type III, congenital dyserythropoietic anemia
Type IIM von Willebrand disease
Type IIN von Willebrand disease