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
|
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.
