Informaţii despre

Nume Osteogenesis Imperfecta, Type Vii
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 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

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Boli A-Z Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Blood Group--Ahonen Blood Group, I System Bone Development Disease Brittle Bone Disorder Bruck Syndrome Caffey Disease Collagen Disease Coxa Vara Dentinogenesis Imperfecta Ehlers-Danlos/osteogenesis Imperfecta Syndrome Ehlers-Danlos Syndrome Ehlers-Danlos Syndrome, Arthrochalasia Type, 1 Ehlers-Danlos Syndrome, Classic Type, 1 Hepatic Adenomas, Familial High Bone Mass Osteogenesis Imperfecta Larsen-Like Syndrome Marfan Syndrome Orthostatic Intolerance Osteochondrodysplasia Osteogenesis Imperfecta, Type I 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 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 Otosclerosis Scleroderma, Familial Progressive Scoliosis Spondyloepiphyseal Dysplasia Congenita Tetraamelia Syndrome, Autosomal Recessive