Informaţii despre

Nume Focal Segmental Glomerulosclerosis 1
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Nephrotic syndrome: Focal and segmental glomerular lesions
Clasificare anatomică Malacards Boli nefrologice (ale rinichilor)
Boli din aceeaşi familie Focal Segmental Glomerulosclerosis 2; Focal Segmental Glomerulosclerosis 3; Focal Segmental Glomerulosclerosis 4; Focal Segmental Glomerulosclerosis 5; Focal Segmental Glomerulosclerosis 6; Focal Segmental Glomerulosclerosis 7; Focal Segmental Glomerulosclerosis 8; Focal Segmental Glomerulosclerosis 9

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Boli A-Z Acromegaly Acute Kidney Tubular Necrosis Acute Lymphocytic Leukemia Acute Promyelocytic Leukemia Adenocarcinoma Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Analbuminemia Aneurysm Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Aplastic Anemia Arteriolosclerosis Arteriovenous Fistula Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atrial Septal Defect 3 Autosomal Dominant Intermediate Charcot-Marie-Tooth 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 C1q Nephropathy Calciphylaxis Charcot-Marie-Tooth Disease Chronic Inflammatory Demyelinating Polyneuropathy Chronic Progressive External Ophthalmoplegia Churg-Strauss Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Crescentic Glomerulonephritis Danubian Endemic Familial Nephropathy Demyelinating Polyneuropathy Denys-Drash Syndrome Desquamative Interstitial Pneumonia Diabetes Mellitus Diffuse Mesangial Sclerosis Donnai-Barrow Syndrome Embryonal Rhabdomyosarcoma Encephalitis Encephalomyopathy Encephalopathy Endotheliitis End Stage Renal Failure Epidermolysis Bullosa Essential Thrombocythemia Familial Glucocorticoid Deficiency 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 Nephrotic Syndrome Familial Partial Lipodystrophy Fanconi Syndrome Focal Segmental Glomerulosclerosis Focal Segmental Glomerulosclerosis 2 Focal Segmental Glomerulosclerosis 3 Focal Segmental Glomerulosclerosis 4 Focal Segmental Glomerulosclerosis 5 Focal Segmental Glomerulosclerosis 6 Focal Segmental Glomerulosclerosis 7 Focal Segmental Glomerulosclerosis 8 Focal Segmental Glomerulosclerosis 9 Frasier Syndrome Galloway-Mowat Syndrome Gitelman Syndrome Glomerulonephritis Graft-Versus-Host Disease Growth Hormone Deficiency Guillain-Barre Syndrome Hematopoietic Stem Cell Transplantation Hepatic Adenomas, Familial Hepatitis Hepatitis B Hepatitis C Hepatitis C Virus Hereditary Wilms' Tumor Herpes Simplex Homozygous Familial Hypercholesterolemia Hydrocephalus, Normal-Pressure Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypercholesterolemia, Autosomal Dominant, 3 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypomelanosis of Ito Hypoparathyroidism Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Interstitial Nephritis Juvenile Rheumatoid Arthritis Kartagener Syndrome Kidney Hypertrophy Kimura Disease Lactic Acidosis Leukemia Lipodystrophy Lipoid Nephrosis Lupus Erythematosus Lymphoma Malignant Hypertension Mantle Cell Lymphoma Marfan Syndrome Mayer-Rokitansky-Kuster-Hauser Syndrome Membranoproliferative Glomerulonephritis Membranous Nephropathy Microcephaly Mitochondrial Encephalomyopathy Myasthenia Gravis Myelodysplastic Syndrome Myelofibrosis Nail-Patella Syndrome Nephrocalcinosis Nephrotic Syndrome Nephrotic Syndrome, Type 1 Neuritis Neurofibromatosis, Type Iv, of Riccardi Neuropathy Obesity-Hypoventilation Syndrome Optic Neuritis Orthostatic Proteinuria Phenylketonuria Pituitary Hormone Deficiency, Combined, 2 Pneumonia Poems Syndrome Polycystic Kidney Disease Polycythemia Polycythemia Vera Polykaryocytosis Inducer Polyneuropathy Polyradiculopathy Primary Biliary Cirrhosis Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 Psoriasis Psoriasis 13 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Sarcoidosis Purpura Rapidly Progressive Glomerulonephritis Renal Adenoma Renal Tubular Acidosis Renovascular Hypertension Retinitis Retinitis Pigmentosa Rhabdomyosarcoma Rhabdomyosarcoma, Embryonal, 1 Rheumatoid Arthritis Riddle Syndrome Sarcoidosis 2 Sensorineural Hearing Loss Sporadic Idiopathic Steroid-Resistant Nephrotic Syndrome with Diffuse Mesangial Sclerosis Sporadic Idiopathic Steroid-Resistant Nephrotic Syndrome with Focal Segmental Hyalinosis Systemic Lupus Erythematosus Takayasu Arteritis Thrombocytopenia Thrombosis Thrombotic Thrombocytopenic Purpura Thymoma Tooth Disease Viral Encephalitis Wilms Tumor 6