Informaţii despre

Nume Renal Osteodystrophy
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Renal osteodystrophy
Clasificare anatomică Malacards Boli nefrologice (ale rinichilor); Boli osoase

Vezi şi

Boli A-Z Achondroplasia Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Arterial Calcification, Generalized, of Infancy, 1 Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Autoimmune Progesterone Dermatitis Axial Osteomalacia 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 Inflammation Disease Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Bone Remodeling Disease Bone Resorption Disease Brachydactyly Calcinosis Calciphylaxis Cervicitis Chondrocalcinosis Chronic Kidney Failure Cohen-Gibson Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Cranial Nerve Palsy Craniodiaphyseal Dysplasia Diffuse Lymphatic Malformation Encephalopathy End Stage Renal Failure Extraskeletal Chondroma Facial Paralysis Familial Hypocalciuric Hypercalcemia Fanconi Anemia, Complementation Group E Fanconi Syndrome Fibrogenesis Imperfecta Ossium Fibrous Dysplasia Giant Cell Tumor Glucocorticoid-Induced Osteoporosis Hepatic Adenomas, Familial Hypercalcemia, Infantile, 1 Hypercalciuria, Absorptive, 2 Hyperostosis Hyperparathyroidism Hyperphosphatemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypervitaminosis D Hypocalcemia, Autosomal Dominant 1 Hypocalciuric Hypercalcemia, Familial, Type Ii Hypoparathyroidism Hypophosphatasia Hypophosphatasia, Adult Hypophosphatemia Hypophosphatemic Rickets, X-Linked Dominant Hypophosphatemic Rickets, X-Linked Recessive Idiopathic Hypercalciuria Immunodeficiency 14 Impaired Renal Function Disease Intracranial Hypertension Ischemic Bone Disease Kummell's Disease Lupus Erythematosus Marchiafava Bignami Disease Mccune-Albright Syndrome Metabolic Acidosis Metaphyseal Chondrodysplasia, Jansen Type Mineral Metabolism Disease Multicentric Carpotarsal Osteolysis Syndrome Multiple Endocrine Neoplasia, Type Iia Myelofibrosis Neuropathy Nontoxic Goiter Occipital Horn Syndrome Oncogenic Osteomalacia Osteitis Fibrosa Osteomalacia Osteonecrosis Osteoporosis Osteoporosis, Juvenile Overhydrated Hereditary Stomatocytosis Paget's Disease of Bone Paget Disease of Bone 5, Juvenile-Onset Pancytopenia Parathyroid Adenoma Parathyroid Carcinoma Parathyroid Gland Disease Periostitis Peritonitis Phosphorus Metabolism Disease Pitt-Hopkins Syndrome Polycystic Kidney Disease Primary Hyperparathyroidism Pseudohypoparathyroidism Pseudohypoparathyroidism, Type Ib Psoriatic Arthritis Pulmonary Alveolar Microlithiasis Renal Hypertension Rickets Sagliker Syndrome Sclerosteosis Sclerosteosis 1 Secondary Hyperparathyroidism of Renal Origin Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Slipped Capital Femoral Epiphysis Spinal Stenosis Spondyloarthropathy Spondylosis Thrombosis Uremia Van Buchem Disease Xanthinuria, Type I