Informaţii despre

Nume Osteogenesis Imperfecta, Type I
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Osteogenesis imperfecta
Clasificare anatomică Malacards Boli bucale; Boli osoase
Boli din aceeaşi familie Osteogenesis Imperfecta, Type Ii; Osteogenesis Imperfecta, Type Iii; Osteogenesis Imperfecta, Type Iv; Osteogenesis Imperfecta, Type Ix; Osteogenesis Imperfecta, Type V; Osteogenesis Imperfecta, Type Vi; Osteogenesis Imperfecta, Type Vii; Osteogenesis Imperfecta, Type Viii; Osteogenesis Imperfecta, Type X; Osteogenesis Imperfecta, Type Xi; Osteogenesis Imperfecta, Type Xii; Osteogenesis Imperfecta, Type Xiii; Osteogenesis Imperfecta, Type Xiv; Osteogenesis Imperfecta, Type Xv; Osteogenesis Imperfecta, Type Xvi; Osteogenesis Imperfecta, Type Xvii

Vezi şi

Boli A-Z Acid-Labile Subunit Deficiency Adie Pupil Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Amelogenesis Imperfecta, Type Iv Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autosomal Dominant Polycystic Kidney Disease Blood Group--Ahonen Bone Development Disease Bone Fracture Bone Remodeling Disease Bone Resorption Disease Brittle Bone Disorder Bruck Syndrome Caffey Disease Cohen-Gibson Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Dental Fluorosis Dentinogenesis Imperfecta Diffuse Idiopathic Skeletal Hyperostosis Ehlers-Danlos/osteogenesis Imperfecta Syndrome Ehlers-Danlos Syndrome, Arthrochalasia Type, 1 Ehlers-Danlos Syndrome, Classic Type, 1 Glucocorticoid-Induced Osteoporosis Hepatic Adenomas, Familial High Bone Mass Osteogenesis Imperfecta Hyperostosis Hyperparathyroidism Immune Suppression Isolated Growth Hormone Deficiency, Type Ib Laron Syndrome Larsen-Like Syndrome Multicentric Carpotarsal Osteolysis Syndrome Nutritional Deficiency Disease Orthostatic Intolerance Osteochondrodysplasia Osteogenesis Imperfecta, Type Ii Osteogenesis Imperfecta, Type Iii Osteogenesis Imperfecta, Type Iv Osteogenesis Imperfecta, Type V Osteogenesis Imperfecta, Type Vi Osteogenesis Imperfecta, Type Vii Osteogenesis Imperfecta, Type Viii Osteoporosis, Juvenile Osteoporotic Fracture Otosclerosis Paroxysmal Extreme Pain Disorder Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities Pituitary Adenoma 1, Multiple Types Polycystic Kidney Disease Pseudohypoparathyroidism Renal Osteodystrophy Saethre-Chotzen Syndrome Scleroderma, Familial Progressive Scoliosis Secondary Adrenal Insufficiency Slipped Capital Femoral Epiphysis Spondyloepiphyseal Dysplasia Congenita Thrombosis Turner Syndrome Vaginitis