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Nume Hyperphosphatemia
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Boli A-Z Acute Kidney Tubular Necrosis Acute Leukemia Aging Albright's Hereditary Osteodystrophy Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Angioid Streaks Aniridia 1 Anorexia Nervosa 1 Arterial Calcification, Generalized, of Infancy, 1 Arterial Calcification of Infancy Arteriovenous Fistula Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 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 Bone Remodeling Disease Bone Resorption Disease Burns Calcinosis Calciphylaxis Cardiac Arrest Chief Cell Adenoma Chronic Kidney Failure Cleft Larynx, Posterior Cohen-Gibson Syndrome Colorectal Cancer Diabetes Mellitus Dyskeratosis Congenita, X-Linked Endotheliitis Familial Hypocalciuric Hypercalcemia Familial Tumoral Calcinosis Fanconi Syndrome Gastroschisis Gitelman Syndrome Headache Hemochromatosis, Type 1 Hinman Syndrome Hypercalcemia, Infantile, 1 Hypercalciuria, Absorptive, 2 Hyperinsulinemic Hypoglycemia, Familial, 6 Hyperostosis Hyperparathyroidism Hyperphosphatemia, Polyuria, and Seizures Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperuricemia Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome Hypervitaminosis D Hypocalcemia, Autosomal Dominant 1 Hypocalciuric Hypercalcemia, Familial, Type Ii Hypoparathyroidism Hypoparathyroidism, Familial Isolated Hypophosphatasia Hypophosphatemia Hypophosphatemic Rickets, Autosomal Dominant Hypophosphatemic Rickets with Hypercalciuria, Hereditary Hypophosphatemic Rickets, X-Linked Dominant Hypophosphatemic Rickets, X-Linked Recessive Hypotrichosis 1 Impaired Renal Function Disease Intussusception Jejunoileitis Lactic Acidosis Leukemia Liver Disease Lymphoblastic Leukemia Metabolic Acidosis Metal Metabolism Disorder Mineral Metabolism Disease Multiple Mitochondrial Dysfunctions Syndrome 5 Myeloma, Multiple Nephrolithiasis Nephrolithiasis, Calcium Oxalate Nephrolithiasis, X-Linked Recessive, with Renal Failure Nephrotic Syndrome Neuronal Intestinal Dysplasia Neuronitis Ocular Motor Apraxia Oncogenic Osteomalacia Osteitis Fibrosa Osteomalacia Parathyroid Adenoma Parathyroid Carcinoma Parathyroid Gland Disease Peritonitis Phosphorus Metabolism Disease Pitt-Hopkins Syndrome Primary Hyperparathyroidism Pseudohypoparathyroidism Pseudohypoparathyroidism, Type Ib Pseudopseudohypoparathyroidism Pulmonary Alveolar Microlithiasis Renal Osteodystrophy Rickets Sclerosteosis Secondary Hyperparathyroidism of Renal Origin Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Spinal Cord Injury Spondylosis T-Cell Leukemia Tracheal Calcification Tumoral Calcinosis, Hyperphosphatemic, Familial Uremia