Informaţii despre

Nume Alpha-Thalassemia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Alpha thalassaemia; Thalassaemia, unspecified
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli de sânge; Boli endocrine; Boli nefrologice (ale rinichilor)
Boli din aceeaşi familie Beta-Thalassemia

Vezi şi

Boli A-Z Acquired Methemoglobinemia Acute Erythroid Leukemia Adie Pupil Adrenocortical Carcinoma, Hereditary Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Thalassemia/mental Retardation Syndrome, Chromosome 16-Related Alpha-Thalassemia/mental Retardation Syndrome, X-Linked Alpha-Thalassemia Myelodysplasia Syndrome Alpha Thalassemia-X-Linked Intellectual Disability Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Androgen Insensitivity Syndrome, Mild Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency Angel-Shaped Phalangoepiphyseal Dysplasia Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Aural Atresia, Congenital Autism X-Linked 2 Beta-Thalassemia Bilirubin Metabolic Disorder Blackwater Fever Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Cerebritis Cerebrovascular Disease Cholelithiasis Chromosomal Triplication Congenital Disorder of Glycosylation, Type Iic Congenital Hemolytic Anemia Congenital Methemoglobinemia Diabetes Mellitus, Insulin-Dependent, 24 Echo Virus 11 Sensitivity Encephalopathy, Ethylmalonic Esophagitis, Eosinophilic, 1 Extrinsic Allergic Alveolitis Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature Fanconi Renotubular Syndrome 1 Fanconi Syndrome Fetal Erythroblastosis Fetal Hemoglobin Quantitative Trait Locus 1 Fetal Hemoglobin Quantitative Trait Locus 6 Gastric Neuroendocrine Tumor Gilbert Syndrome Glucosephosphate Dehydrogenase Deficiency Glutathione Peroxidase Deficiency Glycogen Storage Disease V Heinz Body Anemias Hematopoietic Stem Cell Transplantation Hemoglobin C Disease Hemoglobin E Disease Hemoglobinemia Hemoglobin H Disease Hemoglobinopathy Hemoglobin Zurich Hemolytic Anemia Hepatic Adenomas, Familial Hereditary Persistence of Fetal Hemoglobin-Beta-Thalassemia Syndrome Hereditary Persistence of Fetal Hemoglobin-Sickle Cell Disease Syndrome Hereditary Spherocytosis Hydrops Fetalis Hydrops Fetalis, Nonimmune Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hyper Ige Syndrome Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypochromic Microcytic Anemia Hypospadias Immune Hydrops Fetalis Ischemia Jejunal Atresia Limb Reduction Defect Linear Iga Disease Lissencephaly 1 Liver Angiosarcoma Lutheran Suppressor, X-Linked Malaria Megaloblastic Anemia Methemoglobinemia Methemoglobinemia, Beta-Globin Type Microcytic Anemia Mosaic Trisomy 7 Multiple Mitochondrial Dysfunctions Syndrome 5 Myelodysplastic Syndrome Myelofibrosis Myocardial Infarction Neonatal Anemia Neutrophilic Dermatosis, Acute Febrile Osteochondroma Penis Agenesis Pernicious Anemia Plasmodium Falciparum Malaria Polycythemia Posttransplant Acute Limbic Encephalitis Pseudohermaphroditism Pulmonary Hypertension Purpura Rapp-Hodgkin Syndrome Renal Glucosuria Schimmelpenning-Feuerstein-Mims Syndrome Serpin Peptidase Inhibitor, Clade a, Member 2, Pseudogene Severe Combined Immunodeficiency Sickle Cell Anemia Sickle Cell Disease Spondylitis Spondyloarthropathy 1 Spondyloocular Syndrome Thalassemia Thrombocytosis Urinary System Disease