Informaţii despre

Nume Fanconi Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificare anatomică Malacards Boli nefrologice (ale rinichilor)
Boli din aceeaşi familie Fanconi-Like Syndrome; Primary Fanconi Syndrome

Vezi şi

Boli A-Z 3-Methylglutaconic Aciduria, Type I Acquired Immunodeficiency Syndrome Acquired Monoclonal Ig Light Chain-Associated Fanconi Syndrome Acute Kidney Tubular Necrosis Acute Leukemia Adult-Onset Still's Disease Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Thalassemia Aminoaciduria Amyloidosis Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Bartter Disease Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Brittle Bone Disorder Calciphylaxis Cohen-Gibson Syndrome Congenital Human Immunodeficiency Virus Congenital Hypoplastic Anemia Cystinosis Cystinosis, Late-Onset Juvenile or Adolescent Nephropathic Type Cystinosis, Nephropathic Cystinuria Danubian Endemic Familial Nephropathy Dent Disease 1 Diabetes Insipidus Diabetes Mellitus Diamond-Blackfan Anemia Diarrhea 2, with Microvillus Atrophy Encephalomyopathy Epilepsy Fainting Fanconi-Bickel Syndrome Fanconi-Like Syndrome Fanconi Renotubular Syndrome 1 Focal Segmental Glomerulosclerosis Galactorrhea Galactosemia Gitelman Syndrome Glomerulonephritis Glycogen Storage Disease Growth Hormone Deficiency Heavy Chain Disease Hemoglobinuria Hemosiderosis Hepatitis Hepatitis B Hepatoid Adenocarcinoma Histiocytosis Holoprosencephaly Hydronephrosis Hyperparathyroidism Hyperphosphatemia Hypervitaminosis D Hypoglycemia Hypokalemia Hypoparathyroidism Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypophosphatemia Hypophosphatemic Rickets, X-Linked Dominant Hypophosphatemic Rickets, X-Linked Recessive Ichthyosis Immune-Complex Glomerulonephritis Interstitial Nephritis Isovaleric Acidemia Kearns-Sayre Syndrome Lactic Acidosis Leukemia Liver Cirrhosis Liver Disease Lowe Oculocerebrorenal Syndrome Lymphoblastic Leukemia Lymphoma Lysinuric Protein Intolerance Macroglobulinemia Membranous Nephropathy Metabolic Acidosis Mitochondrial Complex I Deficiency Mitochondrial Encephalomyopathy Mitochondrial Myopathy Mucositis Myeloid Leukemia Myeloma, Multiple Myopathy Nephrocalcinosis Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Nephrotic Syndrome Neurofibromatosis, Type Iv, of Riccardi Obstructive Jaundice Occipital Horn Syndrome Oncogenic Osteomalacia Ossifying Fibroma Osteomalacia Overhydrated Hereditary Stomatocytosis Pancytopenia Paraquat Poisoning Paroxysmal Nocturnal Hemoglobinuria Phenylketonuria Pitt-Hopkins Syndrome Pneumonia Primary Biliary Cirrhosis Primary Fanconi Syndrome Primary Hyperparathyroidism Primary Hypomagnesemia Psoriasis Psoriasis 13 Pulmonary Alveolar Microlithiasis Reflex Sympathetic Dystrophy Renal Dysplasia Renal Glucosuria Renal Osteodystrophy Renal Tubular Acidosis Renal Tubular Transport Disease Retinitis Retinitis Pigmentosa Rickets Saethre-Chotzen Syndrome Sarcoidosis 2 Secondary Hyperparathyroidism of Renal Origin Severe Combined Immunodeficiency Sjogren Syndrome Small Cell Cancer of the Lung Spondylitis Spondyloarthropathy 1 Status Epilepticus Syndrome of Inappropriate Antidiuretic Hormone Thalassemia Thyroiditis Tuberous Sclerosis Tyrosinemia Uremia Uveitis Wissler's Syndrome