Blood Protein Disease,Retinitis Pigmentosa,Roberts-Sc Phocomelia Syndrome,Methemoglobinemia, Beta-Globin Type,Priapism,Spherocytosis, Type 4,Diabetes Mellitus,Splenic Sequestration,Beta-Thalassemia Major,Beta-Thalassemia Intermedia,Thalassemia Minor,Iron Metabolism Disease,Hereditary Elliptocytosis,Spherocytosis, Type 3,Hemoglobin E-Beta-Thalassemia Syndrome,Hemoglobin C-Beta-Thalassemia Syndrome,Splenic Infarction,Hemoglobin Se Disease,Hemoglobin Zurich,Polycythemia,Hemoglobin Lepore-Beta-Thalassemia Syndrome,Hereditary Persistence Of Fetal Hemoglobin-Sickle Cell Disease Syndrome,Hereditary Spherocytosis,Neuropathy, Hereditary Sensory And Autonomic, Type Iib,Sickle Beta Thalassemia,Sickle Cell - Hemoglobin D Disease,Trypanosomiasis,Parasitic Protozoa Infectious Disease,Hemoglobin D Disease,Hemoglobin E Disease,Middle Lobe Syndrome,Cholelithiasis,Hemoglobin C Disease,Hemoglobinopathy,Glucosephosphate Dehydrogenase Deficiency,Sickle Cell Disease,Siderosis,Thalassemia,Hereditary Persistence Of Fetal Hemoglobin-Beta-Thalassemia Syndrome,Kidney Papillary Necrosis,Sickle Cell Disease And Related Diseases,Methemoglobinemia,Hemolytic Anemia,Congenital Hemolytic Anemia,Plasmodium Falciparum Malaria,Deficiency Anemia,Trachoma,Methemoglobinemia, Beta Type,Erythrocytosis, Familial, 6,Beta-Thalassemia, Dominant Inclusion Body Type,Sickle Cell Anemia,Penile Disease,Alpha-Thalassemia,Buruli Ulcer,Acute Chest Syndrome,Hemochromatosis, Type 1,Hemoglobin H Disease,Beta-Thalassemia,Anemia, Sideroblastic, 1,Malaria,Aneruptive Fever,Osteopetrosis, Autosomal Recessive 4,Osteopetrosis, Autosomal Recessive 6,Glutathione Peroxidase Deficiency,Microphthalmia, Syndromic 13,Hypochromic Microcytic Anemia,Autosomal Genetic Disease,Heinz Body Anemias,Fetal Hemoglobin Quantitative Trait Locus 1,Osteopetrosis, Autosomal Recessive 7,Spherocytosis, Type 2,Microcephaly 1, Primary, Autosomal Recessive,Osteopetrosis, Autosomal Recessive 5

Leukemia, Acute Lymphoblastic,Hemoglobinopathy,T-Cell Adult Acute Lymphocytic Leukemia,Adult Acute Lymphocytic Leukemia,Skin Papilloma,Spinal Cord Disease,Alpha-Thalassemia,Hemoglobin H Disease,Urethra Transitional Cell Carcinoma,Heinz Body Anemias

Ventricular Septal Defect,Heart Disease,Physical Disorder,Vascular Disease,Amino Acid Metabolic Disorder,Homocystinuria,Nondisjunction,Methylmalonic Acidemia Without Homocystinuria,Cleft Lip,Fallopian Tube Disease,Placental Abruption,Cleft Lip/Palate,Ophthalmia Neonatorum,Bacterial Conjunctivitis,Male Infertility,Neural Tube Defects, Folate-Sensitive,Rectal Disease,Disorders Of Intracellular Cobalamin Metabolism,Methotrexate Toxicity,Migraine With Aura,Megaloblastic Anemia,Urethritis,Urethral Syndrome,Cardia Cancer,Anus Disease,Homocysteinemia,Methylmalonic Acidemia,Homocystinuria-Megaloblastic Anemia, Cble Complementation Type,Neural Tube Defects,Orofacial Cleft,Vitamin Metabolic Disorder,Vitamin B12 Deficiency,Methylmalonic Aciduria And Homocystinuria Type Cble,Methylmalonic Aciduria And Homocystinuria Type Cblg,Down Syndrome,Autism Spectrum Disorder,Lipoprotein Quantitative Trait Locus,Anencephaly,Myelomeningocele,Chromosomal Duplication Syndrome,Marfan Syndrome,Phenylketonuria

Polycystic Kidney Disease,Methemoglobinemia, Beta-Globin Type,Thalassemia Minor,Alpha Thalassemia-Intellectual Disability Syndrome Type 1,Type 1 Diabetes Mellitus 24,Hemoglobin Zurich,Polycythemia,Splenomegaly,Immune Hydrops Fetalis,Hemoglobinopathy,Sickle Cell Disease,Thalassemia,Methemoglobinemia,Hemolytic Anemia,Congenital Hemolytic Anemia,Histiocytosis-Lymphadenopathy Plus Syndrome,Deficiency Anemia,Neonatal Anemia,Microcytic Anemia,Erythrocytosis, Familial, 7,Sickle Cell Anemia,Alpha-Thalassemia,Hypoglycemic Coma,Hemoglobin H Disease,Beta-Thalassemia,Malaria,Hydrops Fetalis, Nonimmune,Glutathione Peroxidase Deficiency,Hypochromic Microcytic Anemia,Heinz Body Anemias,Alpha-Thalassemia/Mental Retardation Syndrome, Chromosome 16-Related,Hypertension, Essential,Type 1 Diabetes Mellitus 7,Methemoglobinemia, Beta-Globin Type,Iron Deficiency Anemia,Diabetes Mellitus,Stroke, Ischemic,Alpha Thalassemia-Intellectual Disability Syndrome Type 1,Type 1 Diabetes Mellitus 24,Splenomegaly,Type 1 Diabetes Mellitus,Immune Hydrops Fetalis,Hemoglobinopathy,Thalassemia,Methemoglobinemia,Hemolytic Anemia,Deficiency Anemia,Microcytic Anemia,Methemoglobinemia, Alpha Type,Erythrocytosis, Familial, 7,Sickle Cell Anemia,Alpha-Thalassemia,Hypoglycemic Coma,Type 2 Diabetes Mellitus,Hemoglobin H Disease,Beta-Thalassemia,Malaria,Hydrops Fetalis, Nonimmune,Glutathione Peroxidase Deficiency,Hypochromic Microcytic Anemia,Heinz Body Anemias,Alpha-Thalassemia/Mental Retardation Syndrome, Chromosome 16-Related,Hypertension, Essential

X-Linked Recessive Disease,Vascular Disease,Retinitis Pigmentosa,Alzheimer Disease,Primary Ciliary Dyskinesia,Ectodermal Dysplasia,Suppurative Lymphadenitis,Diastolic Heart Failure,Splenic Abscess,Alcoholic Cardiomyopathy,X-Linked Mendelian Susceptibility To Mycobacterial Diseases,Ehrlichiosis,Substance Abuse,Renal Hypertension,Cardiomyopathy, Familial Hypertrophic, 2,Atypical Mycobacteriosis, Familial,Phagocyte Bactericidal Dysfunction,Leukocyte Adhesion Deficiency, Type I,Gastrointestinal Tularemia,Chronic Granulomatous Disease,Disease Of Mental Health,Granulomatous Disease, Chronic, Autosomal Recessive, 4,Granulomatous Disease, Chronic, Autosomal Recessive, 1,Human Granulocytic Anaplasmosis,Immunodeficiency 34,Tuberculous Salpingitis,Immunodeficiency 27b,Malaria,Immune Deficiency Disease,X-Linked Monogenic Disease,Peripheral Artery Disease,Hypertension, Essential,Granulomatous Disease, Chronic, X-Linked,Lung Abscess

Breast Rhabdomyosarcoma,Epidural Abscess,Femoral Neuropathy,Retinitis Pigmentosa,Large Intestine Lipoma,Splenic Sequestration,Anterior Spinal Artery Syndrome,Dieulafoy Lesion,Hemorrhagic Disease,Blood Platelet Disease,Bladder Tuberculosis,Blood Coagulation Disease,Epiglottis Cancer,Inflammatory Liposarcoma,Bilirubin Metabolic Disorder,Fundus Dystrophy,Cerebral Artery Occlusion,Esophageal Diverticulosis,Geotrichosis,Acquired Polycythemia,Hemoglobinopathy,Erythrocytosis, Familial, 8,Perinephritis,Lipoma Of Colon,Folic Acid Deficiency Anemia,Benign Essential Hypertension,Atrophic Vulva,Deficiency Anemia,Cone-Rod Dystrophy 2,Retinitis Pigmentosa 36,Alveolar Soft Part Sarcoma,Lipoprotein Quantitative Trait Locus,Intracranial Berry Aneurysm

Steroid Inherited Metabolic Disorder,Myopathy, Centronuclear, 4,Classic Congenital Adrenal Hyperplasia Due To 21-Hydroxylase Deficiency,Disorder Of Sexual Development,Kohler'S Disease,Familial Glucocorticoid Deficiency,Synostosis,Cortisone Reductase Deficiency,Radioulnar Synostosis,Craniosynostosis,Cytochrome P450 Oxidoreductase Deficiency,Premature Menopause,Amenorrhea,Disordered Steroidogenesis Due To Cytochrome P450 Oxidoreductase Deficiency,46,Xy Sex Reversal,Corneal Dystrophy, Posterior Polymorphous, 1,Crouzon Syndrome,Adrenal Insufficiency, Congenital, With 46,Xy Sex Reversal, Partial Or Complete,Asperger Syndrome,Antley-Bixler Syndrome,Odontochondrodysplasia,Persistent Mullerian Duct Syndrome,Humeroradial Synostosis,Lipoid Congenital Adrenal Hyperplasia,Antley-Bixler Syndrome With Genital Anomalies And Disordered Steroidogenesis,Antley-Bixler Syndrome Without Genital Anomalies Or Disordered Steroidogenesis