Informaţii despre

Nume Mineral Metabolism Disease
Pagina Web www.malacards.org
Clasificare globală Malacards Boli metabolice
Clasificari ICD10 Other disorders of mineral metabolism

Vezi şi

Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Acquired Metabolic Disease Acute Adrenal Insufficiency Acute Thyroiditis Aniridia 1 Anorexia Nervosa 1 Apparent Mineralocorticoid Excess Arterial Calcification of Infancy Arthrogryposis, Distal, Type 3 Autosomal Recessive Hypophosphatemic Rickets Axial Osteomalacia Bartter Disease Bartter Syndrome, Type 2, Antenatal Bartter Syndrome, Type 3 Benign Essential Hypertension Blood Group--Ahonen Bone Remodeling Disease Bone Resorption Disease Calcinosis Calciphylaxis Cell Type Benign Neoplasm Chondrocalcinosis Clear Cell Adenoma Cloacogenic Carcinoma Cohen-Gibson Syndrome Conn's Syndrome Dent Disease 1 Diabetes Insipidus, Nephrogenic, Autosomal Endocrine Organ Benign Neoplasm Enthesopathy Extraskeletal Chondroma Familial Glucocorticoid Deficiency Familial Hypocalciuric Hypercalcemia Familial Tumoral Calcinosis Fanconi-Like Syndrome Fanconi Syndrome Fibrogenesis Imperfecta Ossium Fibrous Dysplasia Gitelman Syndrome Glucocorticoid-Induced Osteoporosis Hyperaldosteronism, Familial, Type I Hypercalcemia, Infantile, 1 Hypercalciuria, Absorptive, 2 Hyperostosis Hyperparathyroidism Hyperphosphatemia Hypervitaminosis D Hypoadrenalism Hypoaldosteronism Hypocalcemia, Autosomal Dominant 1 Hypocalciuric Hypercalcemia, Familial, Type Ii Hypocalciuric Hypercalcemia, Familial, Type Iii Hypokalemia Hypomagnesemia 1, Intestinal Hypoparathyroidism Hypophosphatasia, Adult Hypophosphatemia 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 Invasive Malignant Thymoma Islet Cell Tumor Liver Disease Metaphyseal Chondrodysplasia, Jansen Type Multicentric Carpotarsal Osteolysis Syndrome Multiple Endocrine Neoplasia, Type Iia Nephrocalcinosis Nephrolithiasis Nephrolithiasis, Calcium Oxalate Nontoxic Goiter Oncogenic Osteomalacia Opsismodysplasia Organ System Benign Neoplasm Osteitis Fibrosa Osteogenesis Imperfecta, Type I Osteomalacia Osteoporosis, Juvenile Paget's Disease of Bone Paraneoplastic Syndromes Parathyroid Adenoma Parathyroid Carcinoma Parathyroid Gland Disease Perinephritis Phosphorus Metabolism Disease Premenstrual Tension Primary Hyperparathyroidism Primary Hypomagnesemia Pseudohypoaldosteronism Pseudohypoparathyroidism Pseudohypoparathyroidism, Type Ib Pulmonary Alveolar Microlithiasis Renal Osteodystrophy Renal Tubular Acidosis Renal Tubular Transport Disease Rickets Scleredema Adultorum Sclerosing Hepatic Carcinoma Secondary Hyperparathyroidism of Renal Origin Secondary Hypertrophic Osteoarthropathy Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance Spondylosis Steroid Inherited Metabolic Disorder Subacute Glomerulonephritis Suprasellar Meningioma Taqi Polymorphism Thyroid Crisis Tracheal Calcification Tumoral Calcinosis, Hyperphosphatemic, Familial Tumoral Calcinosis, Normophosphatemic, Familial Uremia Urinary System Disease Xanthinuria, Type I