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Nume Kidney Disease
Pagina Web www.malacards.org
Clasificari ICD10 Disorder of kidney and ureter, unspecified; Renal agenesis, unspecified; Renal hypoplasia, unspecified; Renal tubulo-interstitial disease, unspecified
Clasificare anatomică Malacards Boli nefrologice (ale rinichilor)
Boli din aceeaşi familie Acute Kidney Failure; Chronic Kidney Failure; Renal Infectious Disease

Vezi şi

Boli A-Z Aarskog-Scott Syndrome Acid-Labile Subunit Deficiency Acquired Metabolic Disease Acquired Pure Red Cell Aplasia Acrocallosal Syndrome Acromegaly Acrorenal-Mandibular Syndrome Acute Kidney Failure Acute Kidney Tubular Necrosis Acute Liver Failure Acute Myocardial Infarction Acute Pancreatitis Adenine Phosphoribosyltransferase Deficiency Adenoma Adie Pupil Adrenal Adenoma Aging Al Amyloidosis Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Thalassemia Alport Syndrome and Thin Basement Membrane Nephropathy Alport Syndrome, Autosomal Dominant Alport Syndrome, Autosomal Recessive Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amelogenesis Imperfecta Aminoaciduria Amyloidosis Analbuminemia Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome, Mild Aneurysm Aneurysm of Sinus of Valsalva Angiodysplasia Angiokeratoma of Fordyce Angiomyolipoma Aniridia 1 Anorexia Nervosa 1 Anterolateral Myocardial Infarction Antiphospholipid Syndrome Anuria Aortic Aneurysm Aortic Atherosclerosis Aortitis Apert Syndrome Aplastic Anemia Apnea, Obstructive Sleep Apolipoprotein C-Iii Deficiency Arachnoid Cysts Arachnoiditis Arterial Calcification, Generalized, of Infancy, 1 Arteries, Anomalies of Arteriolosclerosis Arteriosclerosis Arteriovenous Fistula Arteriovenous Malformation Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Asthma Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atrial Fibrillation Atrial Septal Aneurysm Atrial Septal Defect 3 Autonomic Dysfunction Autonomic Neuropathy Autosomal Dominant Polycystic Kidney Disease Autosomal Dominant Tubulointerstitial Kidney Disease Autosomal Dominant Tubulointerstitial Kidney Disease, Umod-Related Bacteriuria Bardet-Biedl Syndrome Barrett Esophagus Bartonellosis Bartter Disease Bestrophinopathy, Autosomal Recessive Bile Duct Cysts Bipolar Disorder Bladder Cancer Blastoma 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 Fracture Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Breast Cancer Brittle Bone Disorder Bronchiectasis Budd-Chiari Syndrome C1q Nephropathy C3 Glomerulopathy Calcinosis Calciphylaxis Cardiac Tamponade Caroli Disease Carotid Artery Disease Carotid Artery Dissection Carotid Intimal Medial Thickness 2 Carpal Tunnel Syndrome Cataract Cellulitis Central Nervous System Lymphoma Central Sleep Apnea Cerebral Aneurysms Cerebral Palsy, Ataxic, Autosomal Recessive Cerebritis Cerebrovascular Disease Cholangiocarcinoma Cholangitis Cholera Cholestasis Chops Syndrome Choroiditis Chromophobe Renal Cell Carcinoma Chromosomal Triplication Chronic Angina Chronic Kidney Failure Chronic Pain Chronic Pyelonephritis Churg-Strauss Syndrome Ciliopathy Clear Cell Papillary Renal Cell Carcinoma Cleft Lip Cohen-Gibson Syndrome Collecting Duct Carcinoma Complement Component 4b Deficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Chloride Diarrhea Congenital Hepatic Fibrosis Congenital Hypothyroidism Congestive Heart Failure Corneal Dystrophy Cornelia De Lange Syndrome Coronary Aneurysm Coronary Artery Anomaly Coronary Artery Dissection, Spontaneous Cortical Blindness Crescentic Glomerulonephritis Critical Limb Ischemia Cryoglobulinemia Cystadenoma Cystic Fibrosis Cystic Kidney Disease Cystic Nephroma Cystinosis Cystinuria Cystitis Danubian Endemic Familial Nephropathy Dementia Dense Deposit Disease Dental Caries Dent Disease 1 Denys-Drash Syndrome Dermal Ridges-off-the-End Dextrocardia Diabetes Insipidus Diabetes Mellitus Diabetic Foot Ulcers Diarrhea Diastolic Heart Failure Differentiated Thyroid Carcinoma Diffuse Lymphatic Malformation Diffuse Mesangial Sclerosis Diffuse Scleroderma Dilated Cardiomyopathy Diverticulitis Donnai-Barrow Syndrome Duodenal Obstruction Duodenitis Dysautonomia Dysostosis Dyspepsia Eclampsia Ecthyma Encephalocele Encephalopathy Endotheliitis End Stage Renal Failure Epidermolysis Bullosa Epidermolysis Bullosa Junctionalis with Pyloric Atresia Epidermolysis Bullosa with Pyloric Atresia Epithelial Recurrent Erosion Dystrophy Esterase C Extrapulmonary Tuberculosis Fabry Disease Factor Xiii Deficiency Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Minimal Changes Familial Juvenile Hyperuricaemic Nephropathy Familial Nephrotic Syndrome Fanconi Anemia, Complementation Group E Fanconi Renotubular Syndrome 1 Fanconi Syndrome Fatty Liver Disease Fecal Incontinence Fibrillary Glomerulonephritis Fibrous Histiocytoma Focal Segmental Glomerulosclerosis Focal Segmental Glomerulosclerosis 1 Frasier Syndrome Frontotemporal Dementia, Chromosome 3-Linked Galactorrhea Galactose Epimerase Deficiency Galloway-Mowat Syndrome Gastric Cancer Genitopatellar Syndrome Germ Cells Tumors Gianotti Crosti Syndrome Gitelman Syndrome Glioma Glomerulonephritis Glucose Intolerance Glucose Transporter Type 1 Deficiency Syndrome Goodpasture Syndrome Gout Growth Hormone Deficiency Hajdu-Cheney Syndrome Headache Heart Disease Helicobacter Pylori Infection Hematuria, Benign Familial Hemoglobinuria Hemolytic-Uremic Syndrome Hemorrhage, Intracerebral Hemosiderosis Henoch-Schoenlein Purpura Hepatic Adenomas, Familial Hepatic Encephalopathy Hepatitis Hepatitis B Hepatitis C Hepatitis C Virus Hepatoblastoma Hepatorenal Syndrome Hereditary Wilms' Tumor Hermansky-Pudlak Syndrome Herpes Zoster Histiocytoma Holoprosencephaly Homocysteinemia Horseshoe Kidney Human Coronavirus Sensitivity Hydrolethalus Syndrome 1 Hydronephrosis Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperglycemia Hyperinsulinemic Hypoglycemia Hyperinsulinism Hyperparathyroidism Hyperphosphatemia Hyperprolactinemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertension, Essential Hypertensive Heart Disease Hypertensive Nephropathy Hypertensive Retinopathy Hyperthyroidism Hyperthyroxinemia, Familial Dysalbuminemic Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypertrophic Pyloric Stenosis Hyperuricemia Hyperuricemic Nephropathy, Familial Juvenile, 1 Hypoaldosteronism Hypoglycemia Hypogonadism Hypokalemia Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypophosphatemia Hyporeninemic Hypoaldosteronism Hypouricemia, Renal, 1 Hypoxia Idiopathic Edema Idiopathic Hypercalciuria Iga Glomerulonephritis Igg4-Related Kidney Disease Immunodeficiency 43 Immunoglobulin E Concentration, Serum Immunotactoid Glomerulopathy Immunotactoid or Fibrillary Glomerulopathy Infertility Inflammatory Bowel Disease Insulin-Like Growth Factor I Insulinoma Interstitial Cystitis Interstitial Nephritis Intracranial Aneurysm Intracranial Cysts Intracranial Hypotension Intrahepatic Cholangiocarcinoma Iron Deficiency Anemia Ischemia Junctional Epidermolysis Bullosa Kartagener Syndrome Keloids Kidney Cancer Kidney Hypertrophy Lactic Acidosis Lattice Corneal Dystrophy Lecithin:cholesterol Acyltransferase Deficiency Left Ventricular Noncompaction Leiomyomatosis Leptospirosis Leukoencephalopathy, Hereditary Diffuse, with Spheroids Limb Ischemia Lipid Metabolism Disorder Lipoid Nephrosis Liver Cirrhosis Liver Disease Logopenic Progressive Aphasia Lung Disease Lupus Erythematosus Luscan-Lumish Syndrome Lymphangioleiomyomatosis Lymphangiomatosis Lymphocele Lymphoma Malaria Male Infertility Malignant Hypertension Malignant Renovascular Hypertension Marchiafava Bignami Disease Marfan Syndrome Maturity-Onset Diabetes of the Young Mayer-Rokitansky-Kuster-Hauser Syndrome Medullary Cystic Kidney Disease 2 Medullary Sponge Kidney Meester-Loeys Syndrome Membranous Nephropathy Metabolic Acidosis Microcytic Anemia Microvascular Complications of Diabetes 3 Miliary Tuberculosis Mineral Metabolism Disease Mitochondrial Myopathy Miyoshi Muscular Dystrophy 1 Moderate and Severe Traumatic Brain Injury Mononeuropathy of the Median Nerve, Mild Mucolipidosis Iii Alpha/beta Mucolipidosis Iii Gamma Multicystic Dysplastic Kidney Multiple Endocrine Neoplasia Multiple Endocrine Neoplasia, Type Iia Multiple Mitochondrial Dysfunctions Syndrome 5 Myelodysplastic Syndrome Myeloma, Multiple Myeloperoxidase Deficiency Myeloproliferative Neoplasm Myocardial Infarction Myocardial Stunning Myopathy Myopathy, Spheroid Body Myxozoa Nail-Patella Syndrome Nasopharyngeal Carcinoma Nasopharyngitis Nephrocalcinosis Nephrogenic Systemic Fibrosis Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Nephronophthisis Nephronophthisis 3 Nephrosclerosis Nephrotic Syndrome Nephrotic Syndrome, Type 1 Neurodegeneration with Brain Iron Accumulation 2a Neurofibroma Neurogenic Bladder Neuronitis Neuropathy Neutropenia Nonalcoholic Steatohepatitis Nonarteritic Anterior Ischemic Optic Neuropathy Non-Immunoglobulin-Mediated Membranoproliferative Glomerulonephritis Occipital Horn Syndrome Oligohydramnios Optic Perineuritis Orbital Cyst Orofaciodigital Syndrome Orofaciodigital Syndrome I Orthostatic Proteinuria Osteogenesis Imperfecta, Type I Osteomalacia Ovarian Cyst Overhydrated Hereditary Stomatocytosis Pachyonychia Congenita 2 Paine Syndrome Pancreatitis Papillary Adenoma Parathyroid Gland Disease Paroxysmal Nocturnal Hemoglobinuria Pediatric Hypertension Peptic Ulcer Disease Pericardial Effusion Pericarditis Periodontal Disease Periodontitis Peripheral Artery Disease Peritonitis Phenylketonuria Pineal Cyst Pitt-Hopkins Syndrome Pituitary Adenoma Pituitary Adenoma 1, Multiple Types Pleuropulmonary Blastoma Pneumonia Poems Syndrome Polycystic Kidney Disease Polycystic Kidney Disease 1 Polycystic Kidney Disease 2 Polycystic Kidney Disease 3 Polycystic Kidney Disease 4 with or Without Hepatic Disease Polycystic Kidney Disease 5 Polycystic Liver Disease Polycystic Liver Disease 1 Polycythemia Polydactyly Polyhydramnios Polymyositis Polyneuropathy Porphyria Portal Hypertension Posterior Urethral Valves Postherpetic Neuralgia Prediabetes Syndrome Pre-Eclampsia Premature Chromatid Separation Trait Priapism Primary Biliary Cirrhosis Primary Effusion Lymphoma Primary Hyperoxaluria Primary Hyperparathyroidism Proliferative Glomerulonephritis Propionic Acidemia Prostatic Cyst Prostatitis Protein Z Deficiency Prune Belly Syndrome Psoriasis Psoriasis 13 Pulmonary Edema Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Hemosiderosis Pure Autonomic Failure Pure Red-Cell Aplasia Purpura Pyelonephritis Pyloric Atresia Pyloric Stenosis Pyruvate Kinase Deficiency of Red Cells Pyuria Radin Blood Group Antigen Rapidly Progressive Glomerulonephritis Recurrent Acute Pancreatitis Relapsing Polychondritis Renal Artery Disease Renal Cysts and Diabetes Syndrome Renal Dysplasia Renal Dysplasia, Cystic Renal Fibrosis Renal Hypertension Renal Hypoplasia Renal Osteodystrophy Renal Pelvis Squamous Cell Carcinoma Renal Tuberculosis Renal Tubular Dysgenesis Renovascular Hypertension Resting Heart Rate, Variation in Restless Legs Syndrome Restrictive Dermopathy, Lethal Reticular Dysgenesis Retinal Degeneration Retinal Detachment Retinal Drusen Retinitis Retinitis Pigmentosa Retroperitoneal Fibrosis Rheumatoid Arthritis Rhombencephalosynapsis Robinow Syndrome Sagliker Syndrome Sarcoidosis 2 Sarcomatoid Renal Cell Carcinoma Scabies Schistosomiasis Secondary Hyperparathyroidism of Renal Origin Seizure Disorder Seminoma Sensorineural Hearing Loss Short-Rib Thoracic Dysplasia 10 with or Without Polydactyly Short-Rib Thoracic Dysplasia 6 with or Without Polydactyly Sickle Cell Anemia Sickle Cell Disease Silent Myocardial Infarction Silicosis Situs Inversus Skin Conditions Sleep Apnea Sleep Disorder Sotos Syndrome 1 Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations Spondyloocular Syndrome Spontaneous Intracranial Hypotension Sporadic Idiopathic Steroid-Resistant Nephrotic Syndrome with Focal Segmental Hyalinosis Squamous Cell Carcinoma Steatocystoma Multiplex Sturge-Weber Syndrome Subdural Empyema Substance Abuse Sudden Sensorineural Hearing Loss Sveinsson Chorioretinal Atrophy Syndrome of Inappropriate Antidiuretic Hormone Synovitis Systemic Lupus Erythematosus Systolic Heart Failure T Cell Deficiency Testicular Cancer Testicular Germ Cell Tumor Testicular Germ Cell Tumor 1 Thalassemia Thrombocytopenia Thrombosis Thyroiditis Tracheal Calcification Transitional Cell Carcinoma Trichohepatoenteric Syndrome 1 Tuberous Sclerosis Tuberous Sclerosis 2 Umbilical Hernia Undifferentiated Embryonal Sarcoma of the Liver Undifferentiated Pleomorphic Sarcoma Unilateral Multicystic Dysplastic Kidney Uremia Uremic Neuropathy Uremic Pruritus Ureteral Obstruction Ureterocele Urethritis Urinary System Disease Urinary Tract Obstruction Vacterl Association Van Der Woude Syndrome 1 Vascular Disease Vasculitis Vesicoureteral Reflux 1 Viral Hepatitis Weber Syndrome West Nile Virus Xanthogranulomatous Pyelonephritis