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Nume Nephrotic Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Nephrotic syndrome: Unspecified
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli de sânge; Boli nefrologice (ale rinichilor)
Boli din aceeaşi familie Familial Nephrotic Syndrome; Nephrotic Syndrome 14; Nephrotic Syndrome 15; Nephrotic Syndrome 16; Nephrotic Syndrome, Type 1; Nephrotic Syndrome, Type 10; Nephrotic Syndrome, Type 11; Nephrotic Syndrome, Type 12; Nephrotic Syndrome, Type 13; Nephrotic Syndrome, Type 2; Nephrotic Syndrome, Type 3; Nephrotic Syndrome, Type 4; Nephrotic Syndrome, Type 6; Nephrotic Syndrome, Type 7; Nephrotic Syndrome, Type 8; Nephrotic Syndrome, Type 9

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Boli A-Z Aarskog-Scott Syndrome Abducens Nerve Disease Acalculous Cholecystitis Acquired Cutis Laxa Acquired Immunodeficiency Syndrome Acrocallosal Syndrome Acrodermatitis Acute Diffuse Nephritis Acute Kidney Tubular Necrosis Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) Acute Myocardial Infarction Acute Poststreptococcal Glomerulonephritis Acute Promyelocytic Leukemia Acute Respiratory Distress Syndrome Adenocarcinoma Adult Respiratory Distress Syndrome Agammaglobulinemia Aging Agnosia Ah Amyloidosis Al Amyloidosis Allergic Hypersensitivity Disease Alopecia Alpha-1-Antitrypsin Deficiency Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Aminoaciduria Amyloidosis Amyloidosis Aa Amyloidosis, Familial Visceral Analbuminemia Androgen Insensitivity Syndrome, Mild Angiomatosis Aniridia 1 Anorexia Nervosa 1 Antithrombin Iii Deficiency Anuria Aphasia Aplastic Anemia Arteries, Anomalies of Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Ascites, Chylous Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Athetosis Atrial Septal Defect 3 Auditory Agnosia Autoimmune Hepatitis Autoimmune Pancreatitis Autosomal Dominant Polycystic Kidney Disease Ayme-Gripp Syndrome Bacillary Angiomatosis Bacteriuria Bardet-Biedl Syndrome Bleeding Disorder, Platelet-Type, 11 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 Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 C1q Nephropathy Calciphylaxis Candida Glabrata Carbuncle Cardiac Tamponade Carotid Artery Thrombosis Castleman Disease Cataract Cavernous Sinus Thrombosis Cecum Adenocarcinoma Cellulitis Cerebellar Degeneration Cerebral Atrophy Cerebral Sinovenous Thrombosis Cerebritis Ceroid Lipofuscinosis, Neuronal, 5 Chickenpox Cholangitis Cholecystitis Cholelithiasis Cholera Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction Chromosome 16p13.3 Deletion Syndrome, Proximal Chronic Graft Versus Host Disease Chronic Neutrophilic Leukemia Chronic Pyelonephritis Chronic Thromboembolic Pulmonary Hypertension Churg-Strauss Syndrome Cicatricial Pemphigoid Cockayne Syndrome Cocoon Syndrome Cold Agglutinin Disease Common Variable Immunodeficiency Compartment Syndrome Complement Deficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Analbuminemia Congenital Nephrotic Syndrome Finnish Type Congenital Portosystemic Shunt Congenital Syphilis Congenital Toxoplasmosis Conjunctivitis Connective Tissue Disease Corneal Dystrophy, Meesmann Crescentic Glomerulonephritis Critical Illness Polyneuropathy Cryofibrinogenemia Cryopyrin-Associated Periodic Syndrome Cryptococcal Meningitis Cryptococcosis Cutis Laxa Cystadenoma Cystic Fibrosis Cystic Kidney Disease Cystinuria Cytomegalovirus Infection Dense Deposit Disease Denys-Drash Syndrome Dermatitis Dermatomyositis Diabetes Insipidus Diabetes Mellitus Diarrhea Diffuse Glomerulonephritis Diffuse Mesangial Sclerosis Disseminated Intravascular Coagulation Dwarfism Dystonia Early Myoclonic Encephalopathy Ehrlichiosis Ellis-Van Creveld Syndrome Embryonal Rhabdomyosarcoma Encephalopathy Endocarditis Endotheliitis End Stage Renal Failure Eosinophilic Gastritis Eosinophilic Gastroenteritis Epidermolysis Bullosa Epidermolysis Bullosa Acquisita Epilepsy Epileptic Encephalopathy, Early Infantile, 3 Epileptic Encephalopathy, Early Infantile, 4 Erdheim-Chester Disease Esophageal Cancer Euthyroid Sick Syndrome Extrapontine Myelinolysis Factor Vii Deficiency Factor X Deficiency Factor Xii Deficiency Familial Hyperlipidemia Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Diffuse Mesangial Proliferation Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Diffuse Mesangial Sclerosis Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Minimal Changes Familial Lcat Deficiency Familial Mediterranean Fever Familial Nephrotic Syndrome Fanconi Anemia, Complementation Group E Fanconi Syndrome Fasciitis Fibrillary Glomerulonephritis Fibromatosis Focal Segmental Glomerulosclerosis Focal Segmental Glomerulosclerosis 1 Food Allergy Fournier Gangrene Frasier Syndrome Galloway-Mowat Syndrome Gastric Adenocarcinoma Gastritis Gastroenteritis Gastrointestinal Stromal Tumor Glomerulonephritis Glomerulopathy with Fibronectin Deposits 2 Glucocorticoid Resistance, Generalized Glutamyl Ribose-5-Phosphate Storage Disease Gonadal Dysgenesis Graft-Versus-Host Disease Granulomatous Hepatitis Graves' Disease Hand, Foot and Mouth Disease Headache Hematopoietic Stem Cell Transplantation Hemolytic-Uremic Syndrome Hemophagocytic Lymphohistiocytosis Hemophilia Hemophilia B Hemosiderosis Hepatic Adenomas, Familial Hepatitis Hepatitis a Hepatitis B Hepatitis C Hepatitis C Virus Hereditary Wilms' Tumor Herpes Zoster Hidradenitis Hidradenitis Suppurativa Horseshoe Kidney Human Coronavirus Sensitivity Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypercholesterolemia, Autosomal Dominant, 3 Hyperostosis Hyperphosphatemia Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Encephalopathy Hyperthyroxinemia, Familial Dysalbuminemic Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypoaldosteronism Hypogonadism Hypolipoproteinemia Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypophosphatasia Hyporeninemic Hypoaldosteronism Hypotonia Ichthyosis Ichthyosis Vulgaris Iga Glomerulonephritis Ige Responsiveness, Atopic Immune-Complex Glomerulonephritis Immunodeficiency 43 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked Immunoglobulin Alpha Deficiency Immunoglobulin E Concentration, Serum Immunotactoid Glomerulopathy Inferior Myocardial Infarction Inflammatory Bowel Disease Inflammatory Myofibroblastic Tumor Influenza Insulin-Like Growth Factor I Interstitial Lung Disease Interstitial Nephritis Intracranial Hypertension Invasive Mole Junctional Epidermolysis Bullosa Kallmann Syndrome Kawasaki Disease Keratomalacia Kidney Hypertrophy Kimura Disease Klippel-Trenaunay-Weber Syndrome Kwashiorkor Late Congenital Syphilis Leishmaniasis Leukemia Leukoencephalopathy, Hereditary Diffuse, with Spheroids Lichen Planus Lichen Planus Pigmentosus Light Chain Deposition Disease Lipid Metabolism Disorder Lipoid Nephrosis Lipoprotein Glomerulopathy Lissencephaly 1 Liver Cirrhosis Loiasis Lung Cancer Lung Disease Lupus Erythematosus Lymphangiectasia, Intestinal Lymphoepithelioma-Like Carcinoma Lymphoepithelioma-Like Thymic Carcinoma Lymphoma Lymphomatoid Papulosis Lymphopenia Lymphoplasmacytic Lymphoma Macroglobulinemia Macular Dystrophy, Corneal Malaria Malignant Mixed Mullerian Tumor Malignant Peritoneal Mesothelioma Mediastinitis Melioidosis Melorheostosis Membranoproliferative Glomerulonephritis Membranous Nephropathy Meningitis Mercury Poisoning Mesangial Proliferative Glomerulonephritis Metabolic Acidosis Metaphyseal Dysplasia, Spahr Type Methylmalonic Aciduria and Homocystinuria, Cblc Type Microcephaly Mixed Connective Tissue Disease Mixed Gonadal Dysgenesis Mouth Disease Multicentric Castleman Disease Multiple Sclerosis Myasthenia Gravis Mycosis Fungoides Myelofibrosis Myeloma, Multiple Myelomeningocele Myocardial Infarction Myocarditis Myxedema Nail-Patella Syndrome Natural Killer Cell Leukemia Necrotizing Fasciitis Nephrocalcinosis Nephronophthisis 2 Nephrotic Syndrome, Type 1 Nephrotic Syndrome, Type 2 Nephrotic Syndrome, Type 3 Neurilemmoma Neurofibroma Neurofibromatosis, Type Ii Neurofibromatosis, Type Iv, of Riccardi Neuromyelitis Optica Neutropenia Neutrophilia, Hereditary Nocardiosis Obstructive Jaundice Ocular Hypertension Oncocytoma Orchitis Osteomyelitis Ovarian Cancer Pancreatic Cystadenoma Pancreatitis Pancytopenia Panniculitis Paraneoplastic Cerebellar Degeneration Paraneoplastic Syndromes Paratyphoid Fever Pericardial Effusion Pericarditis Peritoneal Mesothelioma Peritonitis Pfeiffer Syndrome Phaeohyphomycosis Pierson Syndrome Pigmentary Disorder, Reticulate, with Systemic Manifestations, X-Linked Pituitary Hormone Deficiency, Combined, 2 Pityriasis Rosea Plasma Cell Leukemia Plasmodium Vivax Malaria Plastic Bronchitis Pneumonia Poliomyelitis Polycystic Kidney Disease Polycythemia Polycythemia Vera Polymyositis Polyneuropathy Porphyria Portal Vein Thrombosis Premature Ovarian Failure 7 Primary Intestinal Lymphangiectasia Proliferative Glomerulonephritis Prostate Cancer Prostatitis Protein S Deficiency Pseudohermaphroditism Pulmonary Embolism Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Hemosiderosis Pulmonary Hypertension Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis Purpura Pyelonephritis Pyeloureteritis Cystica Pyuria Rapidly Progressive Glomerulonephritis Recessive Dystrophic Epidermolysis Bullosa Renal Dysplasia Renal Glucosuria Renal Oncocytoma Renal Tubular Acidosis Renovascular Hypertension Retinal Detachment Retinitis Retroperitoneal Fibrosis Rhabdomyosarcoma Rhabdomyosarcoma, Embryonal, 1 Rheumatoid Arthritis Sagittal Sinus Thrombosis Sapho Syndrome Sarcoidosis 2 Schimke Immunoosseous Dysplasia Schistosomiasis Sclerosing Cholangitis Secondary Syphilis Sensorineural Hearing Loss Short Bowel Syndrome Sickle Cell Disease Siderosis Sinusitis Situs Inversus Skin Epithelioid Hemangioma Small Cell Carcinoma Spinal Cord Infarction Splenic Infarction Splenomegaly Spondylitis Spondyloarthropathy Spondyloarthropathy 1 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations Sporadic Idiopathic Steroid-Resistant Nephrotic Syndrome with Diffuse Mesangial Sclerosis Sporadic Idiopathic Steroid-Resistant Nephrotic Syndrome with Focal Segmental Hyalinosis Stiff-Person Syndrome Strongyloidiasis Subacute Bacterial Endocarditis Subacute Glomerulonephritis Sveinsson Chorioretinal Atrophy Synovitis Syphilis Systemic Lupus Erythematosus Systemic Mastocytosis Systemic Scleroderma T Cell Deficiency Temporal Arteritis Teratoma Tetanus Thalassemia Three M Syndrome 1 Thrombocytopenia Thrombocytosis Thrombophilia Thrombosis Thymoma Thyroiditis Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Toxoplasmoză Trehalase Deficiency Trophoblastic Neoplasm Umbilical Hernia Unicentric Castleman Disease Urinary Schistosomiasis Urinary System Disease Van Der Woude Syndrome 1 Varicocele Vasculitis Vibrio Vulnificus Infection Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Weber Syndrome Wilms Tumor 1 Wilms Tumor 6 Xanthogranulomatous Pyelonephritis Yellow Nail Syndrome