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Category:Osteogenesis imperfecta

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<nowiki>osteogénesis imperfecta; üvegcsontúság; osteogenesi inperfektu; osteogènesi imperfecta; Osteogenesis imperfecta; siondróm cnámh briosc; استئوژنز ایمپرفکتا; 成骨不全症; Osteogenesis imperfecta; Osteogenesis İmperfecta; 成骨不全症; osteogenesis imperfecta; פרכת; osteogenesis imperfecta; 成骨不全症; आस्टियोजेनेसिस इम्परफेक्टा; osteogenesis imperfecta; Osteogenesis imperfecta; osteogenesis imperfecta; Osteogenesis imperfecta; osteogenesi imperfetta; ostéogenèse imparfaite; ατελής οστεογένεση; 成骨不全症; Остеогенезис имперфекта; osteogenesis imperfecta; osteogénese imperfeita; Անկատար օստեոգենեզ; Nepilnīgā osteoģenēze; Несовершенный остеогенез; Osteogenesis imperfecta; imperfektna osteogeneza; 骨形成不全症; osteogênese imperfeita; osteogenesis imperfecta; Osteogenesis imperfecta; osteogenesis imperfecta; osteogenesis imperfecta; Büllur xəstəliyi; wrodzona łamliwość kości; ଭଙ୍ଗୁର ଅସ୍ଥି ରୋଗ; 골형성부전증; تێکچوونی دروستبوونی ئێسک; osteoxénese imperfecta; تكون العظم الناقص; osteogenesis imperfecta; bệnh xương thủy tinh; malattia genetica; groupe de maladies; hezur-sistemaren garapenaren sortzetiko akatsa; grup de trastorns genètics que provoquen fragilitat òssia; Krankheit; doença genética; osteohondrodisplazija, pri kateri so zaradi pomanjkanja kolagena tipa I kosti krhke in je okvarjeno vezivno tkivo; osteochondrodysplasia that has material basis in a deficiency in type-I collagen which results in brittle bones and defective connective tissue; genetisk sjukdom; choroba genetyczna; хвороба; group of genetic disorders wey dey result in fragile bones; choroba; מחלת עצמות; trastorno congénito caracterizado por una fragilidad excesiva de las estructuras óseas; perinnöllinen sairaus; doenza conxénita; اضطرابات الجينية; osteochondrodysplasia that has material basis in a deficiency in type-I collagen which results in brittle bones and defective connective tissue; ମନୁଷ୍ୟଙ୍କ ଏକ ରୋଗ; osteogenia imperfecta; huesos de cristal; osteogenesis imperfecta; osteogenese imparfaite; ostéogénose imparfaite; maladie des os de verre; hommes de verre; kristalezko hezurren gaixotasun; Sindrom Vrolik; Penyakit tulang rapuh; Sindrom Ekman-Lobstein; Glasknochenkrankheit; Glasknochen; Glasknochenerkrankung; doença de Ekman-Lobstein; doença de Lobstein; síndrome de Ekman-Lobstein; síndrome de Lobstein; osso de vidro; 脆骨; 玻璃骨; 先天成骨不全症; 玻璃娃娃; 瓷娃娃; 成骨不全; 脆骨症; 脆骨病; Cam kemik hastalığı; OI; Врождённая ломкость костей; Врожденная ломкость костей; Osteogenesis imperfecta; osteogenesis imperfecta; Adair-Dightonov sindrom; osteopsatiroza; bolezen krhkih kosti; ଓଷ୍ଟିଓଜେନେସିସ ଇମ୍ପରଫେକ୍ଟା; osteogenesis imperfecta; samoistna łamliwość kości; sostnienie niezupełne; choroba Vrolika; אוסטיאוגנסיס אימפרפקטה; אוסטאוגנסיס אימפרפקטה; Osteogenesis Imperfecta; אוסטאוגנזה אימפרפקטה; אוסטאוגנזיס אימפרפקטה; Lobstein's syndrome; Vrolik's disease; brittle bone disease; fragilitas ossium; osteopsathyrosis; osteopsathyrosis idiopathica; OI; Lobstein's syndrome; Vrolik's disease; brittle bone disease; fragilitas ossium; osteopsathyrosis; osteopsathyrosis idiopathica; OI; fragilitas ossium; Osteogenesis imperfecta; synnynnäinen sidekudossairaus; OI; osteoxenia imperfecta; Ósos de cristal; osteogenesis imperfecta; csontok törékenysége; osteopsathyrosis; fragilitas ossium; malaltia dels ossos de vidre; síndrome de Lobstein</nowiki>
osteogenesis imperfecta 
osteochondrodysplasia that has material basis in a deficiency in type-I collagen which results in brittle bones and defective connective tissue
osteogenesis imperfecta type V in an adult
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Wikidata Q749409
BNCF Thesaurus ID: 21888
NL CR AUT ID: ph943941
National Library of Spain SpMaBN ID (BNE v1.0): XX553344
J9U entity ID: 987007553341805171
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Subcategories

This category has the following 3 subcategories, out of 3 total.