Category:Osteogenesis imperfecta

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<nowiki>osteogénesis imperfecta; 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; 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; osteogénese imperfeita; osteogenesis imperfecta; bệnh xương thủy tinh; Остеогенезис имперфекта; Nepilnīgā osteoģenēze; Несовершенный остеогенез; Osteogenesis imperfecta; imperfektna osteogeneza; 骨形成不全症; osteogenesis imperfecta; wrodzona łamliwość kości; Osteogenesis imperfecta; osteogenesis imperfecta; osteogenesis imperfecta; Büllur xəstəliyi; ଭଙ୍ଗୁର ଅସ୍ଥି ରୋଗ; 골형성부전증; Անկատար օստեոգենեզ; تێکچوونی دروستبوونی ئێسک; osteoxénese imperfecta; تكون العظم الناقص; osteogenesis imperfecta; 成骨不全症; malattia genetica; hezur-sistemaren garapenaren sortzetiko akatsa; Krankheit; ମନୁଷ୍ୟଙ୍କ ଏକ ରୋଗ; 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; choroba genetyczna; хвороба; osteochondrodysplasia that has material basis in a deficiency in type-I collagen which results in brittle bones and defective connective tissue; choroba; trastorno congénito caracterizado por una fragilidad excesiva de las estructuras óseas; Doença genética; 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; מחלת עצמות; osteogenia imperfecta; huesos de cristal; osteogenesis imperfecta; osteogenese imparfaite; ostéogénose imparfaite; maladie des os de verre; hommes de verre; kristalezko hezurren gaixotasun; malaltia dels ossos de vidre; síndrome de Lobstein; Glasknochenkrankheit; Glasknochen; Glasknochenerkrankung; Doença de ekman-lobstein; Doença de Lobstein; Osso de Vidro; Osteogênese imperfeita; 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; osteogenesis imperfecta; samoistna łamliwość kości; sostnienie niezupełne; choroba Vrolika; אוסטיאוגנסיס אימפרפקטה; אוסטאוגנסיס אימפרפקטה; Osteogenesis Imperfecta; אוסטאוגנזה אימפרפקטה; אוסטאוגנזיס אימפרפקטה; Врождённая ломкость костей; Врожденная ломкость костей; Osteogenesis imperfecta; Sindrom Vrolik; Penyakit tulang rapuh; Sindrom Ekman-Lobstein; ଓଷ୍ଟିଓଜେନେସିସ ଇମ୍ପରଫେକ୍ଟା; Osteogenesis imperfecta; synnynnäinen sidekudossairaus; OI; osteoxenia imperfecta; Ósos de cristal; Lobstein's syndrome; Vrolik's disease; brittle bone disease; Fragilitas ossium; Osteopsathyrosis; osteopsathyrosis; fragilitas ossium; osteogenesis imperfecta; Adair-Dightonov sindrom; osteopsatiroza; bolezen krhkih kosti</nowiki>
成骨不全症 
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
上傳媒體
隸屬於
  • designated intractable/rare disease
  • 罕見病
  • 疾病類別
上級分類
權威檔案
維基數據 Q749409
BNCF: 21888
捷克國家圖書館識別碼: ph943941
西班牙國家圖書館識別碼: XX553344
以色列國家圖書館識別碼: 987007553341805171
在维基数据编辑信息框数据

子分類

此分類包含以下 3 個子分類,共 3 個。

「Osteogenesis imperfecta」分類的媒體檔案

此分類包含以下 18 個檔案,共 18 個。