Megaloblastic Anemia

Informaţii despre

Nume		Megaloblastic Anemia
Pagina Web		www.malacards.org
Clasificare globală Malacards		Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10		Other megaloblastic anaemias, not elsewhere classified
Clasificare anatomică Malacards		Boli de sânge; Boli gastrointestinale; Boli nefrologice (ale rinichilor)
Boli din aceeaşi familie		Megaloblastic Anemia 1

Vezi şi

Boli A-Z		3-Methylglutaconic Aciduria, Type I Acute Leukemia Adie Pupil Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-Thalassemia Al-Raqad Syndrome Anencephaly Aniridia 1 Anorexia Nervosa 1 Aplastic Anemia Arthritis Arthrochalasia Ehlers-Danlos Syndrome Atrial Standstill Atrophic Gastritis Bap1 Tumor Predisposition Syndrome B-Cell Lymphomas Beta-Thalassemia Bleeding Disorder, Platelet-Type, 11 Blind Loop Syndrome Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Brain Small Vessel Disease with or Without Ocular Anomalies Cardiac Conduction Defect Cerebral Folate Deficiency Cerebritis Cervical Spina Bifida Aperta Cervical Spina Bifida Cystica Cervicothoracic Spina Bifida Aperta Cervicothoracic Spina Bifida Cystica Cold Agglutinin Disease Congenital Intrinsic Factor Deficiency Diabetes Mellitus Diffuse Large B-Cell Lymphoma Ebstein Anomaly Encephalopathy Endocarditis Epilepsy Factor Vii Deficiency Fanconi Anemia, Complementation Group E Gastritis Gastroschisis Glutamate Formiminotransferase Deficiency Granulomatous Gastritis Hemolytic Anemia Hemosiderosis Hepatic Adenomas, Familial Hepatitis Hepatitis B Hereditary Spherocytosis Homocysteinemia Homocystinuria Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity Homocystinuria-Megaloblastic Anemia, Cblg Complementation Type Hyperuricemia Hypoascorbemia Immunoglobulin E Concentration, Serum Inherited Metabolic Disorder Ischemic Retinopathy Kwashiorkor Kyasanur Forest Disease Leber Congenital Amaurosis 4 Leukemia Liver Disease Lumbosacral Spina Bifida Aperta Lumbosacral Spina Bifida Cystica Lymphoma Macrocytic Anemia Malaria Marasmus Megaloblastic Anemia 1 Megaloblastic Anemia Due to Dihydrofolate Reductase Deficiency Methylmalonic Aciduria and Homocystinuria, Cblc Type Methylmalonic Aciduria and Homocystinuria Type Cble Methylmalonic Aciduria and Homocystinuria Type Cblg Methylmalonic Aciduria, Cblb Type Monocarboxylate Transporter 1 Deficiency Monogenic Diabetes Myelodysplastic Syndrome Myeloid Leukemia Myelomeningocele Myeloperoxidase Deficiency Neural Tube Defects Neural Tube Defects, Folate-Sensitive Nondisjunction Orotic Aciduria Pancytopenia Pediatric Osteosarcoma Pernicious Anemia Polycythemia Polycythemia Vera Polyneuropathy Psoriasis Psoriasis 13 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pyloric Stenosis Retinitis Sarcoidosis 2 Schizophrenia Schnyder Corneal Dystrophy Splenomegaly Steatorrhea Subacute Bacterial Endocarditis Subacute Cerebellar Degeneration Taeniasis Thalassemia Thiamine-Responsive Megaloblastic Anemia Syndrome Thoracolumbosacral Spina Bifida Aperta Thoracolumbosacral Spina Bifida Cystica Thrombocytopenia Thyroiditis Total Spina Bifida Aperta Total Spina Bifida Cystica Transcobalamin Ii Deficiency Treacher Collins Syndrome 1 Tremor Tropical Sprue Upper Thoracic Spina Bifida Aperta Upper Thoracic Spina Bifida Cystica Vitamin B12 Deficiency Vitamin Metabolic Disorder