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Nume Hypophosphatemia
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Clasificare globală Malacards Boli metabolice

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Boli A-Z Acute Leukemia Acute Liver Failure Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) Acute Myocardial Infarction Acute Pancreatitis Aging Al-Raqad Syndrome Alzheimer Disease 3 Anauxetic Dysplasia 1 Aniridia 1 Ankylosis Anorexia Nervosa 1 Arterial Calcification of Infancy Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Asthma Autism Autosomal Dominant Polycystic Kidney Disease Autosomal Recessive Hypophosphatemic Rickets Autosomal Recessive Non-Syndromic Intellectual Disability Axial Osteomalacia Biliary Atresia Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Bone Remodeling Disease Brittle Bone Disorder Burns Calcinosis Calciphylaxis Cardiac Arrest Cardiac Arrhythmia Cardiogenic Shock Central Pontine Myelinolysis Cohen-Gibson Syndrome Compartment Syndrome Cutaneous-Skeletal Hypophosphatemia Syndrome Dental Fluorosis Dentin Dysplasia Dentin Dysplasia, Type Ii Dentinogenesis Imperfecta Dentinogenesis Imperfecta 1 Diabetes Mellitus Diarrhea Dwarfism Encephalopathy Enthesopathy Ethylene Glycol Poisoning Exfoliation Syndrome Extraskeletal Chondroma Familial Tumoral Calcinosis Fanconi Syndrome Fibrous Dysplasia Head Injury Hemoglobinemia Hemolytic Anemia Hemolytic-Uremic Syndrome Hepatic Adenomas, Familial Hepatitis Hepatitis B Hepatitis C Hepatitis C Virus Hepatocellular Carcinoma Hereditary Hypophosphatemic Rickets Human Coronavirus Sensitivity Hypercalciuria, Absorptive, 2 Hyperglycemia Hyperparathyroidism Hyperphosphatemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypervitaminosis D Hypoglycemia Hypokalemia Hypoparathyroidism Hypophosphatasia Hypophosphatasia, Adult Hypophosphatemic Bone Disease Hypophosphatemic Rickets, Autosomal Dominant Hypophosphatemic Rickets with Hypercalciuria, Hereditary Hypophosphatemic Rickets, X-Linked Dominant Hypophosphatemic Rickets, X-Linked Recessive Idiopathic Hypercalciuria Impaired Renal Function Disease Inappropriate Adh Syndrome Inflammatory Bowel Disease Influenza Lactic Acidosis Legionnaire Disease Legionnaires' Disease Leukemia Liddle Syndrome Liver Cirrhosis Lupus Erythematosus Lymphoblastic Leukemia Lymphoma Macroglobulinemia Macrophage Activation Syndrome Malaria Marfan Syndrome Mccune-Albright Syndrome Meningitis Metabolic Acidosis Mineral Metabolism Disease Mitochondrial Myopathy Monoclonal Paraproteinemia Myeloid Leukemia Myeloma, Multiple Myocardial Infarction Myopathy Nephrocalcinosis Nephrolithiasis Nephrolithiasis/osteoporosis, Hypophosphatemic, 1 Nephrolithiasis, X-Linked Recessive, with Renal Failure Neuroblastoma Neuroleptic Malignant Syndrome Neuropathy Obstructive Jaundice Occipital Horn Syndrome Oncogenic Osteomalacia Opsismodysplasia Osteitis Fibrosa Osteomalacia Osteopetrosis Overhydrated Hereditary Stomatocytosis Pancreatitis Panic Disorder Panostotic Fibrous Dysplasia Paraplegia Parathyroid Gland Disease Pericarditis Periodontitis Peritonitis Phosphorus Metabolism Disease Pitt-Hopkins Syndrome Pneumonia Polycystic Kidney Disease Postural Hypotension Primary Hyperparathyroidism Prostate Cancer Prostatitis Pseudohypoparathyroidism, Type Ib Pulmonary Alveolar Microlithiasis Pulmonary Disease, Chronic Obstructive Q Fever Raine Syndrome Renal Hypodysplasia/aplasia 1 Renal Osteodystrophy Renal Tubular Acidosis Rickets Secondary Hyperparathyroidism of Renal Origin Sudden Infant Death Syndrome Systemic Lupus Erythematosus Three M Syndrome 1 Thrombocytopenia Thymoma Thyrotoxic Periodic Paralysis