Informaţii despre

Nume Rickets
Pagina Web www.malacards.org
Clasificare globală Malacards Boli metabolice; Boli rare
Clasificari ICD10 Rickets, active
Clasificare anatomică Malacards Boli osoase

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Boli A-Z Abetalipoproteinemia Adenoma Adie Pupil Aggressive Periodontitis Aging Alacrima, Achalasia, and Mental Retardation Syndrome Alopecia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Aminoaciduria Anauxetic Dysplasia 1 Andersen Cardiodysrhythmic Periodic Paralysis Angiomatosis Aniridia 1 Anorexia Nervosa 1 Aortic Valve Disease 2 Arterial Calcification of Infancy Arterial Tortuosity Syndrome Arthrochalasia Ehlers-Danlos Syndrome Asphyxiating Thoracic Dystrophy Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autosomal Recessive Hypophosphatemic Rickets Axial Osteomalacia Basal Cell Carcinoma Basal Ganglia Calcification Behr Syndrome 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 Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Bone Remodeling Disease Bone Resorption Disease Brittle Bone Disorder Bronchopulmonary Dysplasia Calcinosis Calciphylaxis Central Precocious Puberty Cerebrotendinous Xanthomatosis Cervicitis Cholestasis Chronic Pyelonephritis Cleidocranial Dysplasia Cohen-Gibson Syndrome Congenital Diarrhea Congenital Ichthyosiform Erythroderma Constipation Cow Milk Allergy Craniosynostosis Crouzon Syndrome with Acanthosis Nigricans Cystinosis Dental Abscess Dermatitis Diabetes Insipidus Diarrhea Digeorge Syndrome Dilated Cardiomyopathy Down Syndrome Dwarfism Enthesopathy Epidermolytic Hyperkeratosis Exfoliation Syndrome Extraskeletal Chondroma Familial Glucocorticoid Deficiency Familial Hypocalciuric Hypercalcemia Fanconi-Bickel Syndrome Fanconi Renotubular Syndrome 1 Fanconi Syndrome Febrile Seizures Fibrous Dysplasia Ganglioneuroblastoma Gastric Dilatation Gastritis Giant Congenital Nevus Glucose/galactose Malabsorption Helix Syndrome Hemangioma Hepatic Adenomas, Familial Hereditary Hypophosphatemic Rickets Histoplasmosis Hypercalciuria, Absorptive, 2 Hyperparathyroidism Hyperphosphatemia Hyperthyroidism Hyperthyroxinemia Hypervitaminosis D Hypoascorbemia Hypocalcemic Vitamin D-Dependent Rickets Hypochondroplasia Hypoparathyroidism Hypophosphatasia Hypophosphatasia, Adult Hypophosphatemia Hypophosphatemic Rickets and Hyperparathyroidism Hypophosphatemic Rickets, Autosomal Dominant Hypophosphatemic Rickets with Hypercalciuria, Hereditary Hypophosphatemic Rickets, X-Linked Dominant Hypophosphatemic Rickets, X-Linked Recessive Hypotonia Ichthyosis Idiopathic Hypercalciuria Impaired Renal Function Disease Impetigo Impetigo Herpetiformis Insulin-Like Growth Factor I Intermediate Uveitis Kallmann Syndrome Kashin-Beck Disease Kwashiorkor Laryngeal Cleft Lipodystrophy, Congenital Generalized, Type 2 Lissencephaly 1 Liver Disease Lymphoma Marasmus Mccune-Albright Syndrome Melanocytic Nevus Syndrome, Congenital Melorheostosis Mesenchymal Cell Neoplasm Microtia Milk Allergy Mineral Metabolism Disease Mitochondrial Complex I Deficiency Mucopolysaccharidosis-Plus Syndrome Multiple Sclerosis Myelofibrosis Nephrocalcinosis Nephrolithiasis Nephrolithiasis, Calcium Oxalate Nephrolithiasis/osteoporosis, Hypophosphatemic, 1 Nephrolithiasis, X-Linked Recessive, with Renal Failure Netherton Syndrome Nevus, Epidermal Nutritional Deficiency Disease Occipital Horn Syndrome Ocular Motor Apraxia Oncogenic Osteomalacia Opsismodysplasia Osteitis Fibrosa Osteoblastoma Osteochondritis Dissecans Osteomalacia Osteomyelitis Osteopetrosis Osteopetrosis, Autosomal Recessive 1 Osteoporosis Overhydrated Hereditary Stomatocytosis Papilledema Parathyroid Adenoma Parathyroid Gland Disease Periodontal Disease Periodontitis Phacomatosis Pigmentokeratotica Phakomatosis Pigmentokeratotica Phenylketonuria Pheochromocytoma Phosphorus Metabolism Disease Pituitary Adenoma 1, Multiple Types Pneumonia Posttransplant Acute Limbic Encephalitis Precocious Puberty Primary Hyperparathyroidism Protein-Losing Enteropathy Pseudohypoparathyroidism Pseudohypoparathyroidism, Type Ii Pulmonary Alveolar Microlithiasis Pycnodysostosis Pyelonephritis Raine Syndrome Ramer Ladda Syndrome Renal Glucosuria Renal Osteodystrophy Renal Tubular Acidosis Rhabdomyosarcoma Sarcoidosis 2 Schimmelpenning-Feuerstein-Mims Syndrome Secondary Hyperparathyroidism of Renal Origin Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Spitz Nevus Spondylitis Spondyloarthropathy 1 Spondyloocular Syndrome Suppurative Periapical Periodontitis Synostosis Three M Syndrome 1 Tracheobronchomalacia Treacher Collins Syndrome 1 Turner Syndrome Tyrosinemia Uremia Urticaria Urticaria Pigmentosa Vitamin D-Dependent Rickets, Type 2a Vitamin D-Dependent Rickets, Type 2b, with Normal Vitamin D Receptor Vitamin D Hydroxylation-Deficient Rickets, Type 1a Vitamin D Hydroxylation-Deficient Rickets, Type 1b Xanthomatosis