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Diseases » Blood conditions » Incidence
 

Incidence Statistics for Types of Blood conditions

The information below shows a list of types of Blood conditions, with information as to the annual incidence of each of these types of Blood conditions. Estimates of the people affected each year are calculated based on the available statistics.

Incidence Statistics for Types of Blood conditions

Disease

Incidence Estimate

US people estimate

Statistic Used for Calculation

Anemia N/A N/A No information
Iron deficiency anemia approx 1 in 24 or 4.12% or 11.2 million people in USA 11,212,400 187,979 annual cases in Victoria 1996 (DHS-VIC); 20% women of childbearing age; 2% adult men (NWHIC)
Sickle cell anemia approx 1 in 34,000 or 0.00% or 8,000 people in USA 8,000 1 per 500 African American births; 1 per 1,000-1,400 Hispanic-American births
Cooley's anemia N/A N/A No information
Aplastic anemia N/A N/A No information
Clotting disorders N/A N/A No information
Hemophilia approx 1 in 680,000 or 0.00% or 400 people in USA 399 about 400 babies annually (NHLBI)
Porphyria N/A N/A No information
Leukemia approx 1 in 8,831 or 0.01% or 30,800 people in USA 30,799 30,800 annual cases in USA (SEER 2002 estimate) including 10,800 lymphocytic, 15,000 myeloid and 5,000 other leukemias; about 29,000 cases annually (NCI); nearly 27,000 adults and more than 2,000 children annually.
Purpura N/A N/A No information
Viral Hemorragic Fevers N/A N/A No information
Hemochromatosis N/A N/A No information
Amyloidosis N/A N/A No information
Autoimmune Hemolytic Anemia approx 1 in 80,000 or 0.00% or 3,400 people in USA 3,399 1 per 80,000 cases to 2.6 per 100,000 (as reported in Rose and Mackay 19981)
Autoimmune Hemophilia N/A N/A No information
Autoimmune Lymphoproliferative Syndrome N/A N/A No information
Autoimmune Thrombocytopenia approx 1 in 10,000 or 0.01% or 27,200 people in USA 27,199 less than 10 per 100,000 cases and 1-4 per 100,000 in children2
Bacteremia N/A N/A No information
Balance disorders N/A N/A No information
Bleeding disorders N/A N/A No information
Circulatory disorder N/A N/A No information
Classic Distal Renal Tubular Acidosis N/A N/A No information
Dialysis-related amyloidosis N/A N/A No information
Favism N/A N/A No information
Hemolytic disease of the newborn N/A N/A No information
Hemolytic uremic syndrome approx 1 in 1,346,534 or 0.00% or 201 people in USA 201 202 cases of postdiarrheal HUS in 28 USA states 2001 (Morbidity and Mortality Weekly Report, 2003)
High Cholesterol N/A N/A No information
Hypercalcemia N/A N/A No information
Hyperkalemia N/A N/A No information
Hyperkalemic Renal Tubular Acidosis N/A N/A No information
Hypoglycemia N/A N/A No information
Hypokalemia N/A N/A No information
Hypotension N/A N/A No information
Immune Thrombocytopenic Purpura N/A N/A No information
Iron deficiency N/A N/A No information
Jaundice N/A N/A No information
Meningococcal disease approx 1 in 108,756 or 0.00% or 2,500 people in USA 2,500 2,501 annual cases notified in USA 1999 (MMWR 1999)
Multiple Myeloma approx 1 in 18,630 or 0.01% or 14,600 people in USA 14,599 14,600 annual cases of multiple myeloma in USA (SEER 2002 estimate)
Myeloma N/A N/A No information
Pernicious anemia N/A N/A No information
Primary amyloidosis N/A N/A No information
Proximal Renal Tubular Acidosis N/A N/A No information
Pulmonary hypertension N/A N/A No information
Renal Tubular Acidosis N/A N/A No information
Septicemia approx 1 in 2,767 or 0.04% or 98,300 people in USA 98,298 1,648 annual cases in Victora 1996 (DHS-VIC)
Sickle Cell Anemia approx 1 in 34,000 or 0.00% or 8,000 people in USA 8,000 1 per 500 African American births; 1 per 1,000-1,400 Hispanic-American births
Thalassemia N/A N/A No information
Thrombocytopenia N/A N/A No information
Thrombosis N/A N/A No information
Von Willebrand disease N/A N/A No information
Acidosis N/A N/A No information
Alkalosis N/A N/A No information
Hyperinsulinemia N/A N/A No information
Hypertension N/A N/A No information
Polycythemia N/A N/A No information
Blood pressure disorders N/A N/A No information
Eclampsia N/A N/A No information
Orthostatic hypotension N/A N/A No information
Preeclampsia N/A N/A No information
Shock N/A N/A No information
Methaemoglobinaemia N/A N/A No information
Serious blood disorders N/A N/A No information
Human carcinogen -- Schistosoma haematobium infection N/A N/A No information
Acute leukemia N/A N/A No information
Chronic leukemia N/A N/A No information
Myelogenous leukemia N/A N/A No information
Hairy cell leukemia N/A N/A No information
Acute lymphocytic leukemia approx 1 in 71,018 or 0.00% or 3,830 people in USA 3,830 3,830 new cases for Acute Lymphocytic Leukemia in the US 2004 (Cancer Facts and Figures, American Cancer Society, 2004)
Acute myeloid leukemia approx 1 in 22,818 or 0.00% or 11,919 people in USA 11,919 11,920 new cases for Acute Myeloid Leukemia in the US 2004 (Cancer Facts and Figures, American Cancer Society, 2004)
Chronic lymphocytic leukemia approx 1 in 33,211 or 0.00% or 8,190 people in USA 8,190 8,190 new cases for Chronic Lymphocytic Leukemia in the US 2004 (Cancer Facts and Figures, American Cancer Society, 2004)
Chronic myeloid leukemia approx 1 in 59,130 or 0.00% or 4,600 people in USA 4,599 4,600 new cases for Chronic Myeloid Leukemia in the US 2004 (Cancer Facts and Figures, American Cancer Society, 2004)
Acute myeloblastic leukemia type 1 N/A N/A No information
Acute myeloblastic leukemia type 2 N/A N/A No information
Acute myeloblastic leukemia type 3 N/A N/A No information
Human T Cell Leukemia Virus 1 N/A N/A No information
Leukemia, T-cell, chronic N/A N/A No information
Philadelphia-negative chronic myeloid leukemia N/A N/A No information
Human T-cell leukemia viruses type 2 N/A N/A No information
Acute leukaemia of ambiguous lineage N/A N/A No information
Acute lymphoblastic leukemia N/A N/A No information
Acute megacaryoblastic leukemia N/A N/A No information
Acute myeloid leukaemia and myelodysplastic syndromes related to alkylating agent N/A N/A No information
Acute myeloid leukaemia and myelodysplastic syndromes related to topoisomerase type II inhibitor N/A N/A No information
Acute myeloid leukaemia and myelodysplastic syndromes, therapy related N/A N/A No information
Metastatic blood cancer N/A N/A No information
Adult T-Cell leukemia N/A N/A No information
Leukemia, mast-cell N/A N/A No information
Blood cancer N/A N/A No information
Adult T-cell leukemia/lymphoma N/A N/A No information
Acute myelocytic leukemia N/A N/A No information
Extramedullary Myeloid Tumor N/A N/A No information
Chloromyeloma N/A N/A No information
Embolism N/A N/A No information
Pulmonary embolism approx 1 in 418 or 0.24% or 650,000 people in USA 650,000 approximately 650,000 cases annually in the USA
Thromboembolism N/A N/A No information
Leukemia, Myeloid, Chronic N/A N/A No information
Chronic Lymphocytic Leukemia, Susceptibility to, 5 N/A N/A No information
Chronic Lymphocytic Leukemia, Susceptibility to, 4 N/A N/A No information
Chronic Lymphocytic Leukemia, Susceptibility to, 3 N/A N/A No information
Chronic Lymphocytic Leukemia, Susceptibility to, 2 N/A N/A No information
Chronic Lymphocytic Leukemia, Susceptibility to, 1 N/A N/A No information
Chronic Lymphocytic Leukemia, Susceptibility to N/A N/A No information
Lymphocytic leukemia N/A N/A No information
Acute lymphoblastic leukemia, Susceptibility to N/A N/A No information
Acute lymphoblastic leukemia, Susceptibility to, 1 N/A N/A No information
Acute lymphoblastic leukemia, Susceptibility to, 2 N/A N/A No information
Chronic Neutrophilic Leukemia N/A N/A No information
Acute basophilic leukaemia N/A N/A No information
Deafness -- lymphoedema -- leukemia N/A N/A No information
Leukemia, Lymphocytic, Acute, L1 N/A N/A No information
Leukemia, Lymphocytic, Acute, L3 N/A N/A No information
Leukemia, Myeloid, Philadelphia-Positive N/A N/A No information
Diabetic Ketoacidosis N/A N/A No information
Neonatal Jaundice N/A N/A No information
Hypobetalipoproteinemia N/A N/A No information
Hemoglobinopathy N/A N/A No information
Pearson's anemia N/A N/A No information
Alpha thalassemia -- silent carrier N/A N/A No information
Alpha thalassemia trait N/A N/A No information
Alpha thalassemia -- Hemoglobin H disease N/A N/A No information
Alpha thalassemia major N/A N/A No information
Beta Thalassemia trait N/A N/A No information
Beta Thalassemia intermedia N/A N/A No information
Fanconi's anemia -- Estren-Dameshek variant N/A N/A No information
Fanconi's anemia -- Complementation group B N/A N/A No information
Fanconi's anemia -- Complementation group C N/A N/A No information
Fanconi's anemia -- Complementation group D1 N/A N/A No information
Fanconi's anemia -- Complementation group D2 N/A N/A No information
Fanconi's anemia -- Complementation group E N/A N/A No information
Fanconi's anemia -- Complementation group F N/A N/A No information
Fanconi's anemia -- Complementation group G N/A N/A No information
Fanconi's anemia -- Complementation group L N/A N/A No information
Fanconi's anemia -- Complementation group I N/A N/A No information
Fanconi's anemia -- Complementation group J N/A N/A No information
Fanconi's anemia -- Complementation group M N/A N/A No information
Fanconi's anemia -- Complementation group N N/A N/A No information
Fanconi's anemia -- Complementation group A N/A N/A No information
Fanconi's anemia N/A N/A No information
Lederer's anemia N/A N/A No information
Spur-cell anemia N/A N/A No information
Achrestic anemia N/A N/A No information
Warm Autoimmune Hemolytic Anemia N/A N/A No information
Cold Autoimmune Hemolytic Anemia N/A N/A No information
Primary Cold Autoimmune Hemolytic Anemia N/A N/A No information
Secondary Cold Autoimmune Hemolytic Anemia N/A N/A No information
Secondary Autoimmune Hemolytic Anemia N/A N/A No information
Primary Autoimmune Hemolytic Anemia N/A N/A No information
Cycloserine-induced Sideroblastic anemia N/A N/A No information
Chloramphenicol-induced Sideroblastic anemia N/A N/A No information
Ethanol-induced Sideroblastic anemia N/A N/A No information
Isoniazid-induced Sideroblastic anemia N/A N/A No information
Drug-induced Sideroblastic anemia N/A N/A No information
Toxin-induced Sideroblastic anemia N/A N/A No information
Sideropenic anemia N/A N/A No information
Myelpathic anemia N/A N/A No information
Hepatocellular jaundice N/A N/A No information
Postoperative septicemia N/A N/A No information
Bacterial septicemia N/A N/A No information
Microcytic hypochromic anemia N/A N/A No information
Megaloblastic anemia N/A N/A No information
Hemolytic anemia N/A N/A No information
Sideroblastic anemia N/A N/A No information
Plasma cell leukemia N/A N/A No information
Systemic Lupus Erythematosus with Hemolytic Anemia, Susceptibility to, 1 N/A N/A No information
Hemolytic Uremic Syndrome, Atypical, Susceptibility to, 6 N/A N/A No information
Hemolytic Uremic Syndrome, Atypical, Susceptibility to, 5 N/A N/A No information
Hemolytic Uremic Syndrome, Atypical, Susceptibility to, 4 N/A N/A No information
Hemolytic Uremic Syndrome, Atypical, Susceptibility to, 3 N/A N/A No information
Hemolytic Uremic Syndrome, Atypical, Susceptibility to, 2 N/A N/A No information
Hemolytic Uremic Syndrome, Atypical, Susceptibility to, 1 N/A N/A No information
Spherocytosis, type 2 N/A N/A No information
Spherocytosis, type 3 N/A N/A No information
Spherocytosis, type 4 N/A N/A No information
Spherocytosis, type 5 N/A N/A No information
Spherocytosis, type 1 N/A N/A No information
Hyperuricaemia N/A N/A No information
Von Willebrand disease, type 3 N/A N/A No information
Von Willebrand disease, type 2N N/A N/A No information
Von Willebrand disease, type 2M N/A N/A No information
Von Willebrand disease, type 2B N/A N/A No information
Von Willebrand disease, type 2A N/A N/A No information
Von Willebrand disease, type 2 N/A N/A No information
Von Willebrand disease, type 1 N/A N/A No information
X-linked sideroblastic anaemia N/A N/A No information
Decreased reticulocyte count N/A N/A No information
Decreased serum phosphate N/A N/A No information
Decreased serum urea N/A N/A No information
Decreased mean cell haemoglobin N/A N/A No information
Decreased mean cell haemoglobin concentration N/A N/A No information
Decreased mean cell volume N/A N/A No information
Decreased oxygen saturation N/A N/A No information
Decreased protein C N/A N/A No information
Decreased protein S N/A N/A No information
Neonatal neutropenia N/A N/A No information
Factor X deficiency N/A N/A No information
Factor X deficiency -- San Antonio N/A N/A No information
Factor X deficiency -- Friuli N/A N/A No information
Factor X deficiency -- Padua N/A N/A No information
Factor X deficiency -- Nottingham N/A N/A No information
Factor X deficiency -- Kanazawa N/A N/A No information
Factor X deficiency -- Shanghai N/A N/A No information
Factor X deficiency -- St. Louis II N/A N/A No information
Factor X deficiency -- Stockton N/A N/A No information
Factor X deficiency -- Taunton N/A N/A No information
Factor X deficiency -- Vorarlberg N/A N/A No information
Factor X deficiency -- Wenatchee I N/A N/A No information
Factor X deficiency -- Wenatchee II N/A N/A No information
Factor X deficiency -- Santo Domingo N/A N/A No information
Factor X deficiency -- Ketchikan N/A N/A No information
Factor X deficiency -- Tokyo N/A N/A No information
Factor X deficiency -- autosomal dominant N/A N/A No information
Normochromic anemia N/A N/A No information
Poikilocytic anemia N/A N/A No information
Normocytic anemia N/A N/A No information
Macrocytic Hyperchromic Anemia N/A N/A No information
Inherited spherocytic anemia N/A N/A No information
Penicillin-induced Immune Hemolytic Anemia N/A N/A No information
Drug-induced Immune Hemolytic Anemia N/A N/A No information
Microcytic Hyperchromic Anemia N/A N/A No information
Doxepine-induced Immune Hemolytic Anemia N/A N/A No information
Microcytic-Normochromic anemia N/A N/A No information
Sulphonamide -induced Immune Hemolytic Anemia N/A N/A No information
Methyldopa-induced Immune Hemolytic Anemia N/A N/A No information
Non-hereditary spherocytic anemia N/A N/A No information
Normocytic-Normochromic anemia N/A N/A No information
Microcytic Anemia N/A N/A No information
Hyperchromic Anemia N/A N/A No information
Macrocytic anemia N/A N/A No information
Type Ia Hyperlipoproteinemia N/A N/A No information
Type Ib Hyperlipoproteinemia N/A N/A No information
Type Ic Hyperlipoproteinemia N/A N/A No information
Type II Hyperlipoproteinemia N/A N/A No information
Hypercholesterolemia, autosomal recessive N/A N/A No information
Homozygous Familial Hypercholesterolemia N/A N/A No information
Chronic anemia N/A N/A No information
Dimorphic anemia N/A N/A No information
Diamond-Blackfan anemia 1 N/A N/A No information
Diamond-Blackfan anemia 2 N/A N/A No information
Diamond-Blackfan anemia 3 N/A N/A No information
Anemia of pregnancy N/A N/A No information
Diamond-Blackfan anemia 4 N/A N/A No information
Diamond-Blackfan anemia 5 N/A N/A No information
Diamond-Blackfan anemia 6 N/A N/A No information
Diamond-Blackfan anemia 7 N/A N/A No information
Diamond-Blackfan anemia 8 N/A N/A No information
Posthemorrhagic anemia N/A N/A No information
Spherocytic anemia N/A N/A No information
Megalocytic-Normochromic anemia N/A N/A No information
Nutritional anemia N/A N/A No information
Quinidine-induced Immune Hemolytic Anemia N/A N/A No information
Cephalosporin-induced Immune Hemolytic Anemia N/A N/A No information
Acid-Base Imbalance N/A N/A No information
Respiratory acidosis N/A N/A No information
Respiratory alkalosis N/A N/A No information
Acquired Aplastic Anemia N/A N/A No information
Acquired idiopathic sideroblastic anaemia N/A N/A No information
Lactic Acidosis N/A N/A No information
Fanconi's syndrome N/A N/A No information
Hemodialysis N/A N/A No information
Volume depletion N/A N/A No information
Dehydration N/A N/A No information
Diseases contagious from blood N/A N/A No information
Diseases contagious from blood transfusion N/A N/A No information
Postoperative Jaundice N/A N/A No information
Hypocalcemia N/A N/A No information
Obstructive Jaundice N/A N/A No information
Acute myeloblastic leukemia type 4 N/A N/A No information
Acute myeloblastic leukemia type 5 N/A N/A No information
Propionic Acidemia N/A N/A No information
Erdheim-Chester Disease N/A N/A No information
Glutaric Acidemia Type II N/A N/A No information
Factor VII deficiency N/A N/A No information
Hyperlipoproteinemia type 2 N/A N/A No information
Pancytopenia N/A N/A No information
Shock, Hypovolaemic N/A N/A No information
Venous Thrombosis N/A N/A No information
Viremia N/A N/A No information
Intracranial Embolism N/A N/A No information
Breast Milk Jaundice approx 1 in 200 or 0.50% or 1.4 million people in USA 1,360,000 0.5%-2.4% of newborns develop breast milk jaundice
Malignant Jaundice N/A N/A No information
Thallessemia N/A N/A No information
Anemias, Sideroblastic N/A N/A No information
Renal failure-like electrolyte imbalances N/A N/A No information
Acid phosphatase elevation N/A N/A No information
Myelomatous polyneuropathy N/A N/A No information
Alkaline phosphatase elevation N/A N/A No information
Folate-deficiency anemia N/A N/A No information
Ehlers-Danlos syndrome with Platelet Dysfunction from Fibronectin Abnormality N/A N/A No information
Methahemoglobinemia N/A N/A No information
Rhesus isoimmunisation N/A N/A No information
Heat cramps N/A N/A No information
Agranulocytosis N/A N/A No information
Neutropenia N/A N/A No information
Deep vein thrombosis N/A N/A No information
Severe fluid retention N/A N/A No information
Transient neutropenia N/A N/A No information
Mild hypercalcemia N/A N/A No information
Mild jaundice N/A N/A No information
Decrease anion gap N/A N/A No information
Decreased bicarbonate N/A N/A No information
Immunoproliferative diseases N/A N/A No information
Hyperprolactinemia N/A N/A No information
Hypolipoproteinemia N/A N/A No information
Acquired amegakaryocytic thrombocytopenia N/A N/A No information
Christmas disease N/A N/A No information
Hemophilia A N/A N/A No information
Hemophilia B N/A N/A No information
The Hemophilias N/A N/A No information
Hemophilic arthropathy N/A N/A No information
Anemia, hypochromic microcytic N/A N/A No information
Hypertensive hypokalemia familial N/A N/A No information
Mental retardation, X-linked -- hypogammaglobulinemia -- progressive neurological deterioration N/A N/A No information
Pregnancy toxemia /hypertension N/A N/A No information
Myeloid Sarcoma N/A N/A No information
Toxemia N/A N/A No information
Anoxemia N/A N/A No information
X-linked alpha thalassemia mental retardation syndrome (ATR-X) N/A N/A No information
Factor XIII deficiency, congenital N/A N/A No information
Factor XIII Deficiency N/A N/A No information
Factor XIII, A1 subunit Deficiency N/A N/A No information
Factor XIII, B subunit Deficiency N/A N/A No information
Factor V and factor VIII, combined deficiency of N/A N/A No information
Hageman factor deficiency N/A N/A No information
Stuart factor deficiency, acquired N/A N/A No information
Stuart factor deficiency, congenital N/A N/A No information
Factor V deficiency N/A N/A No information
Factor 8 deficiency, congenital N/A N/A No information
Factor XI deficiency, congenital N/A N/A No information
Factor V Quebec N/A N/A No information
Factor XII Deficiency N/A N/A No information
Factor IX Deficiency N/A N/A No information
Factor V Leiden mutation N/A N/A No information
Deafness hyperuricemia neurologic ataxia N/A N/A No information
Retinopathy -- aplastic anemia -- neurological abnormalities N/A N/A No information
ATRUS syndrome N/A N/A No information
Hemolytic anemia, acquired autoimmune N/A N/A No information
Heterozygous Beta-thalassemia 1 N/A N/A No information
Heterozygous Beta-thalassemia 2 N/A N/A No information
Hydrops fetalis syndrome due to Beta-thalassemia N/A N/A No information
Leukemia, T-Cell, Acute N/A N/A No information
Portal vein thrombosis N/A N/A No information
Leukemia, Monocytic, Acute N/A N/A No information
Smoldering adult T-Cell leukemia N/A N/A No information
Leukemia, Myeloid, Aggressive-Phase N/A N/A No information
Vitamin K deficiency N/A N/A No information
Hypovolemia N/A N/A No information
Lipoproteinemia N/A N/A No information
Familial Dysbetalipoproteinemia N/A N/A No information
Hyperlipoproteinemia N/A N/A No information
Familial Hypercholesterolemia N/A N/A No information
Platelet function disorders N/A N/A No information
Sickle cell crisis N/A N/A No information
Alpha thalassemia N/A N/A No information
Beta thalassemia N/A N/A No information
Hyperglycemia N/A N/A No information
Methaemoglobinemia N/A N/A No information
Hyperbilirubinemia N/A N/A No information
Coagulopathy N/A N/A No information
Microcytosis N/A N/A No information
Anisocytosis N/A N/A No information
Tularemia N/A N/A No information
Lymphopenia N/A N/A No information
Hypercholesterolemia due to arg3500 mutation of Apo B-100 N/A N/A No information
Hyperinsulinemic hypoglycemia, familial, 1 N/A N/A No information
Hyperinsulinemic hypoglycemia, familial, 2 N/A N/A No information
Hyperinsulinemic hypoglycemia, familial, 3 N/A N/A No information
Hyperinsulinemic hypoglycemia, familial, 4 N/A N/A No information
Hyperinsulinemic hypoglycemia, familial, 5 N/A N/A No information
Hyperinsulinemic hypoglycemia, familial, 7 N/A N/A No information
Leukemia, Myeloid N/A N/A No information
Familial hyperlipoproteinemia type 1 N/A N/A No information
Familial hyperlipoproteinemia type 3 N/A N/A No information
Acute myeloid leukemia, adult N/A N/A No information
Familial hyperlipoproteinemia N/A N/A No information
Anticoagulant poisoning N/A N/A No information
Juvenile myelomonocytic leukemia N/A N/A No information
Sea-Blue histiocytosis N/A N/A No information
T-Lymphocytopenia N/A N/A No information
Congenital spherocytic anemia N/A N/A No information
Severe congenital neutropenia N/A N/A No information
Anemia, Sideroblastic N/A N/A No information
Drug-Induced neutropenia N/A N/A No information
Acute lymphoblastic leukemia, adult N/A N/A No information
Acute myeloblastic leukemia type 6 N/A N/A No information
Acute myeloblastic leukemia type 7 N/A N/A No information
Leukemia, T-Cell N/A N/A No information
Haemoglobinemia N/A N/A No information
Hemoglobinemia N/A N/A No information
Hypophosphatemic rickets N/A N/A No information
Congenital spherocytic hemolytic anemia N/A N/A No information
Neutropenia, severe chronic N/A N/A No information
Galactosemia I N/A N/A No information
Acidemia, methylmalonic N/A N/A No information
Portal thrombosis N/A N/A No information
Leukemia, B-cell, chronic N/A N/A No information
Alba/Geneva I dysfibrinogenemia N/A N/A No information
Adelaide I dysfibrinogenemia N/A N/A No information
Troyes dysfibrinogenemia N/A N/A No information
Saint Louis dysfibrinogenemia N/A N/A No information
Zurich II dysfibrinogenemia N/A N/A No information
Metz dysfibrinogenemia N/A N/A No information
Oslo dysfibrinogenemia N/A N/A No information
Leuven dysfibrinogenemia N/A N/A No information
Vancouver dysfibrinogenemia N/A N/A No information
Bethesda II dysfibrinogenemia N/A N/A No information
Dysfibrinogenemia, familial N/A N/A No information
Asahi I dysfibrinogenemia N/A N/A No information
Oklahoma dysfibrinogenemia N/A N/A No information
Aarhus dysfibrinogenemia N/A N/A No information
Nancy dysfibrinogenemia N/A N/A No information
Baltimore dysfibrinogenemia N/A N/A No information
Paris II dysfibrinogenemia N/A N/A No information
Detroit dysfibrinogenemia N/A N/A No information
Zurich I dysfibrinogenemia N/A N/A No information
Los Angeles dysfibrinogenemia N/A N/A No information
Paris I dysfibrinogenemia N/A N/A No information
Aarau dysfibrinogenemia N/A N/A No information
Bethesda I dysfibrinogenemia N/A N/A No information
Cleveland dysfibrinogenemia N/A N/A No information
Almeria I dysfibrinogenemia N/A N/A No information
Wiesbaden dysfibrinogenemia N/A N/A No information
Parma dysfibrinogenemia N/A N/A No information
Amiens I dysfibrinogenemia N/A N/A No information
Ales dysfibrinogenemia N/A N/A No information
Amsterdam dysfibrinogenemia N/A N/A No information
Aggressive NK-cell leukaemia N/A N/A No information
T-cell prolymphocytic leukemia N/A N/A No information
Familial platelet syndrome with predisposition to acute myelogenous leukemia N/A N/A No information
Leukemia, Lymphocytic, Acute, L2 N/A N/A No information
B-cell prolymphocytic leukaemia N/A N/A No information
Leukemia, Myeloid, Philadelphia-Negative N/A N/A No information
Acute adult T-Cell leukemia N/A N/A No information
Chronic adult T-Cell leukemia N/A N/A No information
Leukemia, Myeloid, Chronic-Phase N/A N/A No information
B-cell chronic lymphocytic leukemia N/A N/A No information
T-cell acute lymphoblastic leukemia N/A N/A No information
Acute erythroleukemia N/A N/A No information
Acute non lymphoblastic leukemia N/A N/A No information
Acute lymphoblastic leukemia congenital sporadic aniridia N/A N/A No information
Chronic myelogenous leukemia N/A N/A No information
Acute promyelocytic leukemia N/A N/A No information
Carotenemia N/A N/A No information
Fungemia N/A N/A No information
Cerebral hemorrhage with amyloidosis, hereditary, Dutch type N/A N/A No information
Onychotrichodysplasia and neutropenia N/A N/A No information
Carotenemia, familial N/A N/A No information
Hypoglycemic attack N/A N/A No information
Diabetic hypoglycemia N/A N/A No information
Hemorrhagic thrombocythemia N/A N/A No information
Essential thrombocytopenia N/A N/A No information
Essential thrombocytosis -- same as essential thrombocythemia N/A N/A No information
Hereditary thrombocythemia N/A N/A No information
IPEX syndrome N/A N/A No information
Polyendocrinopathy, immune dysfunction, and diarrhea, X-linked N/A N/A No information
Enteropathy, autoimmune, with hemolytic anemia and polyendocrinopathy N/A N/A No information
Diarrhea, polyendocrinopathy, fatal infection syndrome, X-linked N/A N/A No information
Immune dysregulation -- polyendocrinopathy -- enteropathy, X linked N/A N/A No information
Diabetes mellitus, congenital insulin-dependent, with fatal secretory diarrhea N/A N/A No information
X-Linked Agammaglobulinemia N/A N/A No information
Wiskott-Aldrich Syndrome N/A N/A No information
Non-ketotic hyperglycemia N/A N/A No information
Leukocyte Adhesion Defect N/A N/A No information
Onychotrichodysplasia, chronic neutropenia and mental retardation syndrome N/A N/A No information
Microcephaly developmental delay pancytopenia N/A N/A No information
Hemolytic anaemia, lethal -- genital anomalies N/A N/A No information
Necrobacillosis N/A N/A No information
Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance N/A N/A No information
Sideroblastic anaemia (generic term) N/A N/A No information
Imerslund's Syndrome N/A N/A No information
Imerslund's Anemia N/A N/A No information
Imerslund-Najman-Grasbeck Anemia N/A N/A No information
Imerslund-Najman-Grasbeck Disease N/A N/A No information
Imerslund-Najman-Grasbeck Syndrome N/A N/A No information
Grasbeck-Imerslund Disease N/A N/A No information
Megaloblastic Anemia 1 N/A N/A No information
Selective Vitamin B12 malabsorption with Proteinuria N/A N/A No information
Juvenile Megaloblastic Anemia N/A N/A No information
Pernicious Anemia, Juvenile type N/A N/A No information
Hyperglycemic Hyperosmolar Nonketotic Syndrome N/A N/A No information
Neonatal sepsis N/A N/A No information
Meningococcemia N/A N/A No information
Postoperative septicaemia N/A N/A No information
Calcification of basal ganglia with or without hypocalcemia N/A N/A No information
Listeriosis sepsis N/A N/A No information
Bicarbonate deficit N/A N/A No information
Myelokathexis syndrome N/A N/A No information
Cardiomyopathy -- spherocytosis N/A N/A No information
Myopathy with lactic acidosis and sideroblastic anemia N/A N/A No information
Mitochondrial myopathy -- lactic acidosis N/A N/A No information
Retinal telangiectasia and hypogammaglobulinemia N/A N/A No information
Renal tubular acidosis, distal N/A N/A No information
Renal tubular acidosis progressive nerve deafness N/A N/A No information
Renal tubular acidosis, distal -- type III N/A N/A No information
Renal tubular acidosis, distal -- type I N/A N/A No information
Renal tubular acidosis, distal, type 4 N/A N/A No information
Renal tubular acidosis, distal, autosomal recessive N/A N/A No information
Neuroaxonal dystrophy -- renal tubular acidosis N/A N/A No information
Renal tubular acidosis, distal, autosomal dominant N/A N/A No information
Histidinuria, renal tubular defect N/A N/A No information
Cholestatic jaundice -renal tubular insufficiency N/A N/A No information
Aleukemic leukemia cutis N/A N/A No information
Prolymphocytic leukemia N/A N/A No information
Leukemia subleukemic N/A N/A No information
Acute biphenotypic leukemia N/A N/A No information
Lymphoblastic lymphoma N/A N/A No information
Large granular lymphocyte leukemia N/A N/A No information
Chronic myelomonocytic leukemia N/A N/A No information
Decreased HBA1c N/A N/A No information
Decreased chloride N/A N/A No information
Hyperkalaemia N/A N/A No information
Hyperlipidaemia N/A N/A No information
Hyperlipidemia in children N/A N/A No information
Hypernatraemia N/A N/A No information
Hyperosmolarity N/A N/A No information
Hyperphosphataemia N/A N/A No information
Navajo poikiloderma N/A N/A No information
Protein S acquired deficiency N/A N/A No information
Electrolyte abnormality N/A N/A No information
Water-Electrolyte Imbalance N/A N/A No information
Franek-Bocker-Kahlen syndrome N/A N/A No information
Microcephaly brain defect spasticity hypernatremia N/A N/A No information
Cyclic neutropenia N/A N/A No information
Methotrexate-associated lymphoproliferative disorders N/A N/A No information
Leukocyte Adhesion Deficiency, Type I N/A N/A No information
Leukocyte Adhesion Deficiency, Type III N/A N/A No information
Leukocyte adhesion deficiency type 1 N/A N/A No information
Leukocyte adhesion deficiency (LAD) N/A N/A No information
Congenital disorder of glycosylation type X -- leukocyte adhesion deficiency syndrome type II phenotype N/A N/A No information
Hypergammaglobulinemia N/A N/A No information
Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality N/A N/A No information
Hypermethioninemia due to S-adenosylhomocysteine hydrolase deficiency N/A N/A No information
Hypofibrinogenemia, congenital N/A N/A No information
Hyponatremia N/A N/A No information
Ornithinemia N/A N/A No information
Pure red cell aplasia, congenital N/A N/A No information
Hypocalcemia, autosomal dominant N/A N/A No information
Granulocytopenia N/A N/A No information
Hypoglycemia with deficiency of glycogen synthetase in the liver N/A N/A No information
Hypermagnesemia N/A N/A No information
Chediak-Higashi Syndrome N/A N/A No information
Galactosemia N/A N/A No information
Classic galactosemia N/A N/A No information
Galactokinase deficiency N/A N/A No information
Familial hyperlipoproteinemia type 4 N/A N/A No information
Hypoalphalipoproteinemia, primary N/A N/A No information
Hypoalphalipoproteinemia (generic term) N/A N/A No information
Abetalipoproteinemia N/A N/A No information
Nephropathy familial with hyperuricemia N/A N/A No information
Hyperlipoproteinemia type 3 N/A N/A No information
Hyperlipoproteinemia type 5 N/A N/A No information
Homozygous hypobetalipoproteinemia N/A N/A No information
Hereditary macrothrombocytopenia N/A N/A No information
Congenital amegakaryocytic thrombocytopenia N/A N/A No information
Capillary leak syndrome with monoclonal gammopathy N/A N/A No information
Hypomagnesemia 4, renal N/A N/A No information
Leukoencephalopathy, arthritis, colitis and hypogammaglobulinemia N/A N/A No information
Hyperprolinemia type 2 N/A N/A No information
X-linked hypogammaglobulinemia N/A N/A No information
Methylmalonic acidemia N/A N/A No information
Hypoprolinemia N/A N/A No information
Familial hypertriglyceridemia N/A N/A No information
Hyperammonemia -- hypoornithinemia -- hypocitrullinemia -- hypoargininemia -- hypoprolinemia N/A N/A No information
Methylmalonic acidemia -- homocystinuria N/A N/A No information
Methylmalonic acidemia, vitamin B12 responsive N/A N/A No information
Acidemia, isovaleric N/A N/A No information
Isovaleric Acidemia N/A N/A No information
Acidemia, propionic N/A N/A No information
Glutaric Acidemia Type I N/A N/A No information
D-glycericacidemia N/A N/A No information
Organic acidemia N/A N/A No information
Refsum disease with increased pipecolic acidemia N/A N/A No information
Tiglic acidemia N/A N/A No information
Succinic acidemia -- lactic acidosis, congenital N/A N/A No information
Succinic acidemia N/A N/A No information
Lactic acidosis, chronic adult form N/A N/A No information
Lactic Acidosis, Fatal Infantile N/A N/A No information
Hypercholesterolemia, autosomal dominant N/A N/A No information
Hyperphenilalaninemia due to pterin-4-alpha-carbinolamine dehydratase deficiency N/A N/A No information
Hypercholesterolemia due to LDL receptor deficiency N/A N/A No information
Multiple carboxylase deficiency, propionic acidemia N/A N/A No information
Magnesium wasting renal N/A N/A No information
Prekallikrein deficiency, congenital N/A N/A No information
Lactic acidosis congenital infantile N/A N/A No information
Isovaleric academia N/A N/A No information
Propionic academia N/A N/A No information
Hyperhomocysteinemia N/A N/A No information
Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl N/A N/A No information
Methylmalonicacidemia with homocystinuria, cbl D N/A N/A No information
Pyruvate kinase deficiency, hemolytic anemia N/A N/A No information
Methylmalonic acidemia, Methylmalonyl CoA mutase deficiency N/A N/A No information
Methylmalonic acidemia, methylmalonyl CoA racemase deficiency N/A N/A No information
Hyperlysinemia, persistent N/A N/A No information
Citrullinemia I, later-onset N/A N/A No information
Valinemia N/A N/A No information
Periodic hyperlysinemia N/A N/A No information
Pyruvate Kinase Deficiency N/A N/A No information
Hyperprolinemia type II N/A N/A No information
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome N/A N/A No information
Tyrosinemia N/A N/A No information
Citrullinemia II N/A N/A No information
Galactosemia III N/A N/A No information
Tyrosinemia, type III N/A N/A No information
Hyperprolinemia type I N/A N/A No information
Citrullinemia I N/A N/A No information
Protein C deficiency N/A N/A No information
Tyrosinemia Type I N/A N/A No information
The Methylmalonic Acidemias N/A N/A No information
Inherited Hemolytic-Uremic Syndrome N/A N/A No information
Diphosphoglycerate mutase deficiency of erythrocyte N/A N/A No information
Adenosine triphosphatase deficiency, anemia due to N/A N/A No information
Adenosine triphosphatase deficiency, anaemia due to N/A N/A No information
ADP platelet receptor P2Y12, deficiency of N/A N/A No information
Adenylate Kinase Deficiency N/A N/A No information
Agammaglobulinemia N/A N/A No information
Primary agammaglobulinemia N/A N/A No information
X-linked agammaglobulinaemia N/A N/A No information
Agammaglobulinemias, Primary N/A N/A No information
Agammaglobulinemia, microcephaly, and severe dermatitis N/A N/A No information
Agammaglobulinemia, autosomal recessive N/A N/A No information
Agammaglobulinemia, non-Bruton type N/A N/A No information
Agammaglobulinemia, X-linked, type 2 N/A N/A No information
Agammaglobulinemia, alymphocytotic type N/A N/A No information
Hypogammaglobulinemia due to CD19 deficiency N/A N/A No information
Hypobetalipoproteinaemia -- ataxia -- hearing loss N/A N/A No information
Congenital thrombotic disease due to protein C deficiency N/A N/A No information
Homozygous protein C deficiency N/A N/A No information
Protein S deficiency N/A N/A No information
Hemoglobin E disease N/A N/A No information
Macrothrombocytopenia -- progressive deafness N/A N/A No information
Choroideremia -- hypopituitarism N/A N/A No information
Hyperglycinemia N/A N/A No information
Familial chronic benign neutropenia N/A N/A No information
Chronic benign neutropenia N/A N/A No information
Hypophosphatemia, Familial N/A N/A No information
Idiopathic adult neutropenia N/A N/A No information
Hypophosphatemia N/A N/A No information
Severe acute neutropenia N/A N/A No information
Idiopathic chronic severe neutropenia N/A N/A No information
Chronic autoimmune neutropenia N/A N/A No information
Hemoglobin C Thalassemia N/A N/A No information
Hemoglobin SC N/A N/A No information
Hemoglobin S-G (S-D) N/A N/A No information
Hemoglobin C homozygous (CC) N/A N/A No information
Hemoglobin D Homozygous (DD) N/A N/A No information
Hemoglobin S/hemoglobin Lepore, Boston N/A N/A No information
Hemoglobin E homozygous N/A N/A No information
Hemoglobin S/hemoglobin O, Arab N/A N/A No information
Hemoglobin, constant spring N/A N/A No information
Hemoglobin H N/A N/A No information
Hereditary methemoglobinemia, recessive, type II N/A N/A No information
Hereditary methemoglobinemia, recessive N/A N/A No information
Aplastic anemia -- paroxysmal nocturnal hemoglobinuria syndrome N/A N/A No information
Plasmacytoma anaplastic N/A N/A No information
Heterocellular hereditary persistence of fetal hemoglobin, Swiss type N/A N/A No information
Hereditary persistence of fetal hemoglobin N/A N/A No information
Hemoglobin F, Hereditary persistence of, heterocellular N/A N/A No information
Hemoglobin F, Hereditary persistence of, pancellular N/A N/A No information
Hemoglobinuria N/A N/A No information
Hemoglobin C disease N/A N/A No information
Paroxysmal Nocturnal Hemoglobinuria N/A N/A No information
Methemoglobinemia, beta-globin type N/A N/A No information
Thalassemia minima N/A N/A No information
Arcobacter butzleri infection N/A N/A No information
Arcobacter cryaerophilus infection N/A N/A No information
Arcobacter infection N/A N/A No information
Hyperimmunoglobinemia D with recurrent fever N/A N/A No information
Serratia sepsis N/A N/A No information
Congenital disorder of glycosylation type X -- Bombay blood group phenotype N/A N/A No information
Hypomagnesemia with hypocalciuria N/A N/A No information
Familial hypertryptophanemia N/A N/A No information
Hereditary hyperuricemia N/A N/A No information
Hyperornithinemia N/A N/A No information
Hyperpipecolatemia N/A N/A No information
Hypocalciuric hypercalcemia, familial, type 2 N/A N/A No information
Hypocalciuric hypercalcemia, familial, type 1 N/A N/A No information
Hypocalciuric hypercalcemia, familial, type 3 N/A N/A No information
Tumor lysis syndrome N/A N/A No information
Heavy-chain diseases N/A N/A No information
Hypocalciuric hypercalcemia, familial N/A N/A No information
Antithrombin Deficiency, type I N/A N/A No information
Antithrombin Deficiency, type II N/A N/A No information
Antithrombin Deficiency N/A N/A No information
Antithrombin III deficiency, congenital N/A N/A No information
Acquired prothrombin deficiency N/A N/A No information
Acquired hypoprothrombinemia N/A N/A No information
Prothrombin deficiency N/A N/A No information
Fanconi like syndrome N/A N/A No information
Congenital Antithrombin III Deficiency N/A N/A No information
Primary granulocytic sarcoma N/A N/A No information
Glanzmann Thrombasthenia N/A N/A No information
Defibrination syndrome N/A N/A No information
Fibrinogen deficiency, congenital N/A N/A No information
Familial primary cryofibrinogenemia N/A N/A No information
Cryofibrinogenemia N/A N/A No information
Hypofibrinogenemia, familial N/A N/A No information
Congenital Afibrinogenemia N/A N/A No information
Anemia, Hemolytic, Warm Antibody N/A N/A No information
Hypertryptophanemia N/A N/A No information
Anemia, Blackfan Diamond N/A N/A No information
Hyperchylomicronemia N/A N/A No information
Dyserythropoietic anemia, congenital N/A N/A No information
Hyperprolinaemia type I N/A N/A No information
Refractory anaemia with ringed sideroblasts N/A N/A No information
Hemolytic anaemia due to adenylate kinase deficiency N/A N/A No information
Hemolytic anemia due to adenylate kinase deficiency N/A N/A No information
Polycythemia vera N/A N/A No information
Dyslipidemia N/A N/A No information
Thrombocythemia N/A N/A No information
Cryoglobulinemia N/A N/A No information
Histidinemia N/A N/A No information
Choroideremia N/A N/A No information
Carnosinemia N/A N/A No information
Waldenstrom macroglobulinemia N/A N/A No information
Maternal hyperphenylalaninemia N/A N/A No information
Vancomycin resistant enterococcal bacteremia N/A N/A No information
X-linked sideroblastic anemia N/A N/A No information
Familial hyperchylomicronemia N/A N/A No information
Hepatorenal tyrosinemia N/A N/A No information
Cooley syndrome N/A N/A No information
Essential mixed cryoglobulinemia N/A N/A No information
Diamond-Blackfan anemia N/A N/A No information
Hereditary spherocytic hemolytic anemia N/A N/A No information
Cold antibody hemolytic anemia N/A N/A No information
Warm-reacting-antibody hemolytic anemia N/A N/A No information
Non-ketotic hyperglycinemia N/A N/A No information
Hereditary non-spherocytic hemolytic anemia N/A N/A No information
Oculocutaneous tyrosinemia N/A N/A No information
Agammaglobulinemia -- microcephaly -- craniosynostosis -- severe dermatitis N/A N/A No information
Deafness-tubular acidosis-anaemia N/A N/A No information
Warm-reacting-antibody haemolytic anemia N/A N/A No information
Von Willebrand disease, recessive form N/A N/A No information
Willebrand disease, acquired N/A N/A No information
Von Willebrand disease, dominant form N/A N/A No information
WHIM syndrome N/A N/A No information
Sarcosinemia N/A N/A No information
Hyperglycerolemia, infantile form N/A N/A No information
Hyperimmunoglobulinemia E N/A N/A No information
Hyperglycerolemia, adult form N/A N/A No information
Sideroblastic anemia, hereditary N/A N/A No information
Hyperglycerolemia N/A N/A No information
Thiamine responsive megaloblastic anemia syndrome N/A N/A No information
Hyperglycerolemia, juvenile form N/A N/A No information
Dyserythropoietic anemia, congenital type 1 N/A N/A No information
Dyserythropoietic anemia, congenital type 2 N/A N/A No information
Dyserythropoietic anemia, congenital type 3 N/A N/A No information
Sideroblastic anemia, autosomal N/A N/A No information
Fanconi anemia type C N/A N/A No information
Dilutional hyponatremia N/A N/A No information
Anemia, Iron-Deficiency N/A N/A No information
Anemia, Neonatal N/A N/A No information
Combined hyperlipidemia, familial N/A N/A No information
Atransferrinemia N/A N/A No information
Sitosterolemia N/A N/A No information
Hypomagnesemia primary N/A N/A No information
Hypoglycemia, leucine-induced N/A N/A No information
Galactorrhoea-Hyperprolactinaemia N/A N/A No information
Hyperphenylalaninemia with primapterinuria N/A N/A No information
Renal hypouricemia N/A N/A No information
Hypoketonemic hypoglycemia N/A N/A No information
Congenital aplastic anemia N/A N/A No information
Adenosine deaminase, elevated, hemolytic anemia due to N/A N/A No information
Congenital analbuminemia N/A N/A No information
Debler anemia N/A N/A No information
Acatalasemia N/A N/A No information
Acanthocytosis N/A N/A No information
Anaemia due to pyrimidine 5' nucleotidase deficiency N/A N/A No information
Anaemia, sideroblastic, X-linked -- ataxia N/A N/A No information
Anemia, Refractory, with Excess of Blasts N/A N/A No information
Anemia, Refractory, with Excess of Blasts, type 1 N/A N/A No information
Anemia, Refractory, with Excess of Blasts, type 2 N/A N/A No information
Familial dysalbuminemic hyperthyroxinemia N/A N/A No information
Hypomagnesemia caused by selective magnesium malabsorption N/A N/A No information
Bisalbuminemia N/A N/A No information
Bisalbuminemia, acquired N/A N/A No information
Hyperostosis-hyperphosphatemia syndrome N/A N/A No information
Hypomagnesemia with normocalciuria N/A N/A No information
X-linked dyserythropoietic anaemia and thrombocytopenia N/A N/A No information
Bisalbuminemia, inherited N/A N/A No information
Hypernatremia N/A N/A No information
Polycythemia rubra N/A N/A No information
Thrombocytosis N/A N/A No information
Spherocytosis N/A N/A No information
Langerhans Cell Histiocytosis N/A N/A No information
Acquired agranulocytosis N/A N/A No information
Hereditary spherocytosis N/A N/A No information
Xerocytosis, heriditary N/A N/A No information
Spherocytic hereditary elliptocytosis N/A N/A No information
Multicentric reticulohistiocytosis N/A N/A No information
Mild hereditary elliptocytosis N/A N/A No information
Hereditary pyropoikilocytosis N/A N/A No information
Di Guglielmo I -- acute N/A N/A No information
Di Guglielmo I -- chronic N/A N/A No information
Stomatocytic hereditary elliptocytosis N/A N/A No information
Mild hereditary elliptocytosis in infancy N/A N/A No information
Hereditary elliptocytosis N/A N/A No information
Hemophagocytic lymphohistiocytosis, familial, 2 N/A N/A No information
Hemophagocytic lymphohistiocytosis, familial, 3 N/A N/A No information
Hemophagocytic lymphohistiocytosis, familial, 4 N/A N/A No information
Hemophagocytic lymphohistiocytosis, familial, 1 N/A N/A No information
Hemophagocytic Lymphohistiocytosis N/A N/A No information
Overhydrated hereditary stomatocytosis N/A N/A No information
Histiocytosis, Non-Langerhans-Cell N/A N/A No information
Familial erythrocytosis, 1 N/A N/A No information
Familial erythrocytosis, 2 N/A N/A No information
Elliptocytosis 1 N/A N/A No information
Familial erythrocytosis, 3 N/A N/A No information
Familial erythrocytosis, 4 N/A N/A No information
Erythropoietic Protoporphyria N/A N/A No information
Protoporphyria erythropoietic N/A N/A No information
Porphyria, congenital erythropoietic N/A N/A No information
Anemia, sideroblastic spinocerebellar ataxia N/A N/A No information
Myelocerebellar disorder N/A N/A No information
Cope's syndrome N/A N/A No information
Thrombotic thrombocytopenic purpura, congenital N/A N/A No information
Thrombotic thrombocytopenic purpura, acquired N/A N/A No information
Thrombasthenia N/A N/A No information
Thrombocytopenic purpura, autoimmune N/A N/A No information
Henoch-Schonlein purpura N/A N/A No information
Arthralgia -- purpura -- weakness syndrome N/A N/A No information
Acute panmyelosis with myelofibrosis N/A N/A No information
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, And Calvarial Hyperostosis N/A N/A No information
Dursun Syndrome N/A N/A No information
Chronic Idiopathic Myelofibrosis N/A N/A No information
Wolman Disease with Hypolipoproteinemia and Acanthocytosis N/A N/A No information
Hyperreninemic Hypoaldosteronism, Familial 2 N/A N/A No information
Abuelo Forman Rubin Syndrome N/A N/A No information
Chronic Myeloproliferative Disease, Unclassified N/A N/A No information
CML-Like Syndrome, Familial N/A N/A No information
Epstein's Syndrome N/A N/A No information
Thrombocytopenia -- Multiple Congenital Anomalies N/A N/A No information
Pearson's marrow-pancreas syndrome N/A N/A No information
Alport syndrome -- mental retardation -- midface hypoplasia -- elliptocytosis N/A N/A No information
Alport syndrome with macrothrombocytopenia N/A N/A No information
Alport Syndrome N/A N/A No information
Amegakaryocytic thrombocytopenia N/A N/A No information
Hereditary primary Fanconi disease N/A N/A No information
Fanconi syndrome N/A N/A No information
Phocomelia -- thrombocytopenia -- encephalocele -- urogenital malformation N/A N/A No information
Blood coagulation disorders, inherited N/A N/A No information
Chronic neutropenia N/A N/A No information
Fanconi pancytopenia N/A N/A No information
Neutropenia -- monocytopenia -- deafness N/A N/A No information
Familial myelofibrosis N/A N/A No information
Acute cholinergic dysautonomia N/A N/A No information
Acute myelofibrosis N/A N/A No information
Acute myelosclerosis N/A N/A No information
Acute panmyelosis N/A N/A No information
Alport syndrome with leukocyte inclusions and macrothrombocytopenia N/A N/A No information
Skeletal and Cardiac Malformations with thrombocytopenia N/A N/A No information
Skeleto cardiac syndrome with thrombocytopenia N/A N/A No information
Absent T lymphocytes N/A N/A No information
Quebec platelet disorder N/A N/A No information
Platelet disorder, familial, with associated myeloid malignancy N/A N/A No information
Congenital nonhemolytic jaundice N/A N/A No information
Thrombocytopenia -- cerebellar hypoplasia -- short stature N/A N/A No information
Von Willebrand disease, platelet type N/A N/A No information
White platelet syndrome N/A N/A No information
Storage pool platelet disease N/A N/A No information
Storage pool platelet deficiency, SPD N/A N/A No information
Gray platelet syndrome N/A N/A No information
Tidal platelet dysgenesis N/A N/A No information
Acquired Pure Red Cell Aplasia N/A N/A No information
Thrombocytopathy N/A N/A No information
Red cell phospholipid defect with hemolysis N/A N/A No information
Pure red cell aplasia N/A N/A No information
Hypokalemic periodic paralysis N/A N/A No information
Hyperkalemic periodic paralysis N/A N/A No information
Hemolytic uremic syndrome, atypical, childhood N/A N/A No information
D-minus hemolytic uremic syndrome (D-HUS) -- pregnancy related N/A N/A No information
D-plus hemolytic uremic syndrome (D+HUS) N/A N/A No information
Atypical hemolytic uremic syndrome N/A N/A No information
D-minus hemolytic uremic syndrome (D-HUS) -- familial N/A N/A No information
Shwachman-Diamond Syndrome N/A N/A No information
Hyperosmolar hyperglycemic nonketotic syndrome N/A N/A No information
Angioimmunoblastic with dysproteinemia lymphadenopathy N/A N/A No information
Myelofibrosis-osteosclerosis N/A N/A No information
Monoclonal gammopathy of undetermined significance N/A N/A No information
Letterer-Siwe disease N/A N/A No information
Hyperbilirubinemia transient, familial, neonatal N/A N/A No information
Catastrophic Antiphospholipid Syndrome N/A N/A No information
Unusual facies, Myelodysplasia and immunodeficiency N/A N/A No information
Erythroblastosis fetalis N/A N/A No information
Non-diarrheal (D-) HUS syndrome N/A N/A No information
Fetal and neonatal alloimmune thrombocytopenia N/A N/A No information
Human monocytic ehrlichiosis N/A N/A No information
Heparin-induced thrombocytopenia N/A N/A No information
Multiple sclerosis -- ichthyosis -- factor 8 deficiency N/A N/A No information
Thrombocytopenia -- chromosome breakage N/A N/A No information
Thrombocytopathy -- asplenia -- miosis N/A N/A No information
Thrombocytopenia X-linked N/A N/A No information
Thrombocytopenia -- Robin sequence N/A N/A No information
Primary tubular proximal acidosis N/A N/A No information
Disorder of Cornification 12 (Neutral Lipid Storage Type) N/A N/A No information
Anemic -- hematuria syndrome N/A N/A No information
Holoprosencephaly, recurrent infections, and monocytosis N/A N/A No information
Cystic fibrosis -- gastritis -- megaloblastic anaemia N/A N/A No information
Unusual facies, mental retardation, short stature, hemolytic anemia and delayed puberty N/A N/A No information
Lymphadenopathy, angioimmunoblastic with dysproteinemia N/A N/A No information
Hyperferritinemia, hereditary with congenital cataracts N/A N/A No information
Onycho-tricho-dysplasia -- neutropenia N/A N/A No information
Lazy leukocyte syndrome N/A N/A No information
Rhnull syndrome N/A N/A No information
Hydrops fetalis -- anaemia -- immune disorder -- absent thumb N/A N/A No information
Hypercoagulability syndrome, due to glycosylphosphatidylinositol deficiency N/A N/A No information
Loeffler's endocarditis N/A N/A No information
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency N/A N/A No information
Blast crisis N/A N/A No information
Aantibodies anti-FVIIIc syndrome N/A N/A No information
Hemangioma thrombocytopenia syndrome N/A N/A No information
Mc Leod neuroacanthocytosis syndrome N/A N/A No information
Rh deficiency syndrome N/A N/A No information
Hemolytic jaundice N/A N/A No information
Tetany N/A N/A No information
Myelodysplastic syndromes approx 1 in 19,428 or 0.01% or 14,000 people in USA 14,000 14,000 people are diagnosed with myelodysplastic syndrome each year in the US (American Cancer Society, Medical News Today)
Myeloproliferative diseases N/A N/A No information
DIC N/A N/A No information
Leukocyte Disorders N/A N/A No information
Thombocytopenia X-linked N/A N/A No information
Kernicterus N/A N/A No information
Felty Syndrome N/A N/A No information
ATR16 N/A N/A No information
Aase syndrome 2 N/A N/A No information
Aase Smith syndrome N/A N/A No information
Aase-Smith I syndrome N/A N/A No information
Banti's syndrome N/A N/A No information
Aase Syndrome N/A N/A No information
May-Hegglin Anomaly N/A N/A No information
Bernard-Soulier Syndrome N/A N/A No information
Banti Syndrome N/A N/A No information
Chronic Myeloproliferative Disorders N/A N/A No information
Thrombocytopenia, cyclic N/A N/A No information
Revesz Debuse syndrome N/A N/A No information
Low birth weight -- dwarfism -- dysgammaglobulinemia N/A N/A No information
Retinopathy -- anaemia- CNS anomalies N/A N/A No information
Revesz Syndrome N/A N/A No information
Vaquez disease N/A N/A No information
Osler-Vaquez disease N/A N/A No information
Owren Parahemophilia N/A N/A No information
Cutler Syndrome N/A N/A No information
May-Hegglin thrombocytopenia N/A N/A No information
Fibronectin-Deficient EDS N/A N/A No information
Trichomegaly cataract hereditary spherocytosis N/A N/A No information
Isoimmune neonatal neutropenia N/A N/A No information
Erdheim-Chester syndrome N/A N/A No information
Majeed syndrome N/A N/A No information
Richter syndrome N/A N/A No information
Schnitzler syndrome N/A N/A No information
Rietti-Greppi-Micheli syndrome N/A N/A No information
Sarrouy disease N/A N/A No information
Schridde syndrome N/A N/A No information
Smith disease N/A N/A No information
Stryker-Halbeisen syndrome N/A N/A No information
Zieve syndrome N/A N/A No information
EGE N/A N/A No information
Heiner syndrome N/A N/A No information
Korovnikov syndrome N/A N/A No information
Mosse syndrome N/A N/A No information
O'Higgins disease N/A N/A No information
Portsmouth syndrome N/A N/A No information
Postperfusion syndrome N/A N/A No information
Complement component 2 deficiency N/A N/A No information
Hypocomplementemic urticarial vasculitis N/A N/A No information
Complement receptor deficiency N/A N/A No information
Erythroblastopenia N/A N/A No information
Asrar-Facharzt-Haque syndrome N/A N/A No information
Immune thrombocytopenia N/A N/A No information
Bone-Marrow failure syndromes N/A N/A No information
Acral dysostosis -- dyserythropoiesis N/A N/A No information
Complement component deficiency N/A N/A No information
Acquired pure megakaryocytic aplasia N/A N/A No information
Lemierre's syndrome N/A N/A No information
Cold agglutination syndrome N/A N/A No information
Hemophagocytic reticulosis N/A N/A No information
Kotzot-Richter syndrome N/A N/A No information
Bing-Neel syndrome N/A N/A No information
Blum's syndrome N/A N/A No information
ALL-Down syndrome N/A N/A No information
Bamberger albuminuria (obsolete term) N/A N/A No information
Benjamin syndrome N/A N/A No information
Bernard syndrome N/A N/A No information
Blue and bloated syndrome N/A N/A No information
Blueberry muffin syndrome N/A N/A No information
Comly syndrome N/A N/A No information
Dana syndrome N/A N/A No information
Disequilibrium syndrome N/A N/A No information
Estren-Dameshek syndrome N/A N/A No information
Gasser-Karrer syndrome N/A N/A No information
Panostotic fibrous dysplasia N/A N/A No information
Transient erythroblastopenia of childhood N/A N/A No information
Myeloid splenomegaly N/A N/A No information
Say syndrome N/A N/A No information
Hoyeraal-Hreidarsson syndrome N/A N/A No information
Jacobsen syndrome N/A N/A No information
Plasminogen activitor inhibitor type 1 deficiency, congenital N/A N/A No information
Ghosal syndrome N/A N/A No information
Cystic fibrosis -- gastritis -- megaloblastic anemia N/A N/A No information
ATR-X syndrome N/A N/A No information
Thong-Douglas-Ferrante syndrome N/A N/A No information
Fanconi-ichthyosis-dysmorphism N/A N/A No information
Myelodysplastic/myeloproliferative disease N/A N/A No information
Paris-Trousseau thrombocytopenia N/A N/A No information
Plasminogen deficiency, congenital N/A N/A No information
Hemolytic anemia, lethal -- genital anomalies N/A N/A No information
Thrombomodulin anomalies, familial N/A N/A No information
Sebastian syndrome N/A N/A No information
Retinopathy -- anemia -- CNS anomalies N/A N/A No information
Deal-Barratt-Dillon syndrome N/A N/A No information
Schlegelberger-Grote syndrome N/A N/A No information
Oslam syndrome N/A N/A No information
TAU syndrome N/A N/A No information
Sackey-Sakati-Aur syndrome N/A N/A No information
Faye-Petersen-Ward-Carey syndrome N/A N/A No information
Idiopathic hypereosinophilic syndrome N/A N/A No information
Short stature -- hyperkaliemia -- acidosis N/A N/A No information
Gardner-Morrisson-Abbot syndrome N/A N/A No information
Neutropenia intermittent N/A N/A No information
Goldstein-Hutt syndrome N/A N/A No information
Semmerkrot-Haraldsson-Weenaes syndrome N/A N/A No information
Baber's syndrome N/A N/A No information
Arakawa's syndrome 2 N/A N/A No information
Pelger-Huet anomaly N/A N/A No information
Fitzgerald-Williams-Flaujeac trait N/A N/A No information
Myelofibrosis N/A N/A No information
Meadows syndrome N/A N/A No information
Pseudopolycythaemia N/A N/A No information
Epstein (C.J.) syndrome N/A N/A No information
Kostmann syndrome N/A N/A No information
Marchiafava-Micheli disease N/A N/A No information
Rosai-Dorfman disease N/A N/A No information
Evan's syndrome N/A N/A No information
Dressler (D.)syndrome N/A N/A No information
Levine-Critchley syndrome N/A N/A No information
Hypereosinophilic syndrome N/A N/A No information
Plummer-Vinson syndrome N/A N/A No information
WT limb blood syndrome N/A N/A No information
Fechtner syndrome N/A N/A No information
Weatherall syndrome N/A N/A No information
TAR syndrome N/A N/A No information
Hand-Schuller-Christian Syndrome N/A N/A No information

Types of Blood conditions

For more information about types of Blood conditions, refer to our section on types of Blood conditions.

About incidence:

The medical term 'incidence' of Blood conditions usually refers to the annual diagnosis rate of new cases of Blood conditions. Prevalence is a different medical disease measure that refers to the estimated population of people who are managing Blood conditions at any given time (e.g. prevalence includes people who have had a medical condition for a long time). For more information on prevalence and incidence statistics, see about prevalence and incidence statistics.



Footnotes:
1. The Autoimmune Diseases, Noel R. Rose, Ian R. Mackay, 1998
2. Rose and Mackay, 1998, The Autoimmune Diseases, Third Edition
 

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