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Nume Hypokalemia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli metabolice
Clasificari ICD10 Hypokalaemia

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Boli A-Z Acute Adrenal Insufficiency Acute Diarrhea Acute Lymphocytic Leukemia Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) Adenocarcinoma Adenoma Adenoma of the Pancreas Adrenal Adenoma Adrenal Cortex Disease Adrenal Gland Disease Aging Alcohol Abuse Aldosterone-Producing Adenoma Alport Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Antenatal Bartter Syndrome Anuria Apparent Mineralocorticoid Excess Appendicitis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Distal, Type 3 Asthma Atrial Fibrillation Atrial Septal Defect 4 Atrioventricular Block Autoinflammation with Infantile Enterocolitis Autosomal Dominant Polycystic Kidney Disease Back Pain Bartter Disease Bartter Syndrome, Type 2, Antenatal Bartter Syndrome, Type 3 Bartter Syndrome, Type 4a, Neonatal, with Sensorineural Deafness Bartter Syndrome, Type 4b, Neonatal, with Sensorineural Deafness Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brain Injury Breast Cancer Brugada Syndrome Burns Cardiac Arrest Cardiac Arrhythmia Central Pontine Myelinolysis Cholera Chondrocalcinosis Coffin-Lowry Syndrome Colitis Colonic Pseudo-Obstruction Compartment Syndrome Congenital Disorder of Glycosylation, Type Iic Congestive Heart Failure Conn's Syndrome Constrictive Pericarditis Corticosteroid-Binding Globulin Deficiency Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Cutaneous Anthrax Cystic Fibrosis Dengue Virus Dent Disease 1 Diabetes Insipidus Diabetes Insipidus, Nephrogenic, Autosomal Diabetes Insipidus, Neurohypophyseal Diabetes Mellitus Diarrhea Early Repolarization Associated with Ventricular Fibrillation Eating Disorder Encephalopathy Endocrine Organ Benign Neoplasm Endotheliitis Enterocolitis Enterovesical Fistula Extrapontine Myelinolysis Familial Glucocorticoid Deficiency Familial Hypertension Familial Periodic Paralysis Fanconi Syndrome Fibromuscular Dysplasia Ganglioneuroblastoma Gastric Cancer Gitelman Syndrome Glomerulonephritis Glucose Intolerance Head Injury Hemangiopericytoma, Malignant Hemochromatosis, Neonatal Hemolytic Anemia Hepatic Adenomas, Familial Hepatic Coma Hepatic Encephalopathy Hepatitis Hepatorenal Syndrome Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperaldosteronism, Familial, Type I Hypercalciuria, Absorptive, 2 Hyperglycemia Hyperparathyroidism Hypertension, Diastolic Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Retinopathy Hyperthyroidism Hyperuricemia Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome Hypoaldosteronism Hypoglycemia Hypokalemic Alkalosis, Familial, with Specific Renal Tubulopathy Hypokalemic Periodic Paralysis, Type 1 Hypoparathyroidism Hypophosphatemia Hyporeninemic Hypoaldosteronism Idiopathic Edema Inappropriate Adh Syndrome Inclusion Body Myositis Infantile Bartter Syndrome with Sensorineural Deafness Intracranial Hypertension Ischemia Islet Cell Tumor Kidney Disease Leishmaniasis Leptospirosis Leukemia Liddle Syndrome Long Qt Syndrome Lung Cancer Lymphoblastic Leukemia Malaria Malignant Hypertension Membranoproliferative Glomerulonephritis Metabolic Acidosis Mineral Metabolism Disease Mucositis Multidrug-Resistant Tuberculosis Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly Myeloid Leukemia Myocardial Infarction Myopathy Myositis Nephrocalcinosis Nephrolithiasis Nephrolithiasis, Calcium Oxalate Nephrolithiasis, X-Linked Recessive, with Renal Failure Neurodegeneration with Brain Iron Accumulation 2a Neuroendocrine Tumor Neuropathy Obstructive Jaundice Ocular Motor Apraxia Orthostatic Proteinuria Osteomalacia Pancreatic Adenoma Pancreatic Cholera Pancreatic Neuroendocrine Tumor Pancreatitis Paraplegia Paraquat Poisoning Pendred Syndrome Pericarditis Peritonitis Pheochromocytoma Pituitary Carcinoma Polycystic Kidney Disease Polyhydramnios Polyneuropathy Prostatitis Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak Pseudohypoaldosteronism Pseudohypoaldosteronism, Type I, Autosomal Dominant Pseudohypoaldosteronism, Type I, Autosomal Recessive Quadriplegia Rapp-Hodgkin Syndrome Renal Artery Disease Renal Artery Obstruction Renal Hypertension Renal Tubular Acidosis Renal Tubular Dysgenesis Renal Tubular Transport Disease Right Bundle Branch Block Second-Degree Atrioventricular Block Secretory Diarrhea Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance Septal Myocardial Infarction Short Bowel Syndrome Small Cell Carcinoma Spinal Cord Injury Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations Status Asthmaticus Steroid Inherited Metabolic Disorder Strongyloidiasis Suprasellar Meningioma Syncope Syndrome of Inappropriate Antidiuretic Hormone Thrombocytopenia Thyroiditis Thyrotoxic Periodic Paralysis Thyrotoxic Periodic Paralysis 2 Traumatic Brain Injury Tremor Ulcerative Colitis Ureteral Disease Vipoma Wdha Syndrome Zollinger-Ellison Syndrome