Informaţii despre

Nume Hereditary Spherocytosis
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Hereditary spherocytosis
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli de sânge
Boli din aceeaşi familie Spherocytosis, Type 1; Spherocytosis, Type 2; Spherocytosis, Type 3; Spherocytosis, Type 4; Spherocytosis, Type 5

Vezi şi

Boli A-Z Acrocallosal Syndrome Acute Erythroid Leukemia 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 Al-Raqad Syndrome Androgen Insensitivity Syndrome, Mild Anemia, Congenital Dyserythropoietic, Type Ii Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency Angioid Streaks Aniridia 1 Anorexia Nervosa 1 Aplastic Anemia Arthrochalasia Ehlers-Danlos Syndrome Ataxia Neuropathy Spectrum Beta-Adrenergic Stimulation, Response to Beta-Thalassemia Blood Group--Ahonen Blood Group, Dombrock System Blood Group Incompatibility Blood Group, I System Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism Central Retinal Vein Occlusion Cerebritis Cholelithiasis Cholestasis Coarctation of Aorta Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Disorder of Glycosylation, Type Iic Congenital Dyserythropoietic Anemia Congenital Hemolytic Anemia Congenital Nonspherocytic Hemolytic Anemia Congestive Heart Failure Corneal Dystrophy, Avellino Type Crigler-Najjar Syndrome, Type Ii Diabetes Mellitus, Transient Neonatal, 1 Dubin-Johnson Syndrome Elliptocytosis 2 Encephalitis Encephalopathy Epb42-Related Hereditary Spherocytosis Epithelial Recurrent Erosion Dystrophy Erythema Infectiosum Evans' Syndrome Factor V Deficiency Familial Adenomatous Polyposis Fetal Erythroblastosis Fetal Hemoglobin Quantitative Trait Locus 1 Follicular Lymphoma Ganglioneuroma Gilbert Syndrome Glucosephosphate Dehydrogenase Deficiency Glyceraldehyde-3-Phosphate Dehydrogenase Deficiency Hantavirus Pulmonary Syndrome Hematopoietic Stem Cell Transplantation Hemoglobin C Disease Hemoglobin E Disease Hemoglobin H Disease Hemoglobinopathy Hemoglobinuria Hemolytic Anemia Hepatitis Hepatitis C Hereditary Elliptocytosis Hereditary Persistence of Fetal Hemoglobin-Beta-Thalassemia Syndrome Hereditary Persistence of Fetal Hemoglobin-Sickle Cell Disease Syndrome Hinman Syndrome Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Encephalopathy Hypertrophic Cardiomyopathy Interstitial Lung Disease Intrahepatic Cholestasis Ischemic Optic Neuropathy Kernicterus Leukemia Loeys-Dietz Syndrome 3 Lung Disease Lymphoma Macular Dystrophy, Retinal, 1, North Carolina Type Malaria Mediastinitis Megaloblastic Anemia Moyamoya Disease 1 Multiple Acyl-Coa Dehydrogenase Deficiency Myoclonic-Astastic Epilepsy Neonatal Jaundice Neuropathy Overhydrated Hereditary Stomatocytosis Pancreatitis Pancytopenia Paroxysmal Nocturnal Hemoglobinuria Parvovirus Antenatal Infection Patent Foramen Ovale Pfeiffer Syndrome Pigmented Purpuric Eruption Pneumonia Polycythemia Polycythemia Vera Portal Vein Thrombosis Posttransplant Acute Limbic Encephalitis Priapism Protein C Deficiency Protein S Deficiency Pulmonary Embolism Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Hypertension Purpura Pyelonephritis Pyoderma Pyoderma Gangrenosum Pyridoxine-Responsive Sideroblastic Anemia Pyropoikilocytosis, Hereditary Pyruvate Kinase Deficiency of Red Cells Rapp-Hodgkin Syndrome Renal Tubular Acidosis Retinal Vein Occlusion Retinitis Retinohepatoendocrinologic Syndrome Rh-Null, Regulator Type Roberts Syndrome Sickle Cell Anemia Sickle Cell Disease Silicosis Spherocytosis, Type 1 Spherocytosis, Type 2 Spherocytosis, Type 3 Spherocytosis, Type 4 Spherocytosis, Type 5 Spinal Cord Disease Spinal Cord Infarction Splenic Infarction Splenic Sequestration Splenomegaly Stuttering Tetraamelia Syndrome, Autosomal Recessive Thalassemia Thoracoabdominal Syndrome Thrombocytopenia Thrombocytosis Thrombosis Thrombotic Thrombocytopenic Purpura Trichomegaly Viral Pneumonia Vitamin B12 Deficiency Wandering Spleen Wilms Tumor 6 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome