Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition A moderately severe form of osteogenesis imperfecta characterized by increased bone fragility and low bone mass that clinically manifests from infancy as susceptibility to bone fractures, short stature, mild to moderate scoliosis in most, gray-blue or white sclera, and dentinogenesis imperfecta. Disease data Classification Clinical subtype Synonyms OI type 4 OI typu 4 ORPHA code 216820 OMIM code 616507 ICD10 code Q78.0 ICD11 code LD24.K0 *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl