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Category:Osteogenesis imperfecta

<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; 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; bệnh xương thủy tinh; 골형성부전증; 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; Անկատար օստեոգենեզ; تێکچوونی دروستبوونی ئێسک; osteoxénese imperfecta; تكون العظم الناقص; osteogenesis imperfecta; osteogénese imperfeita; trastorno congénito caracterizado por una fragilidad excesiva de las estructuras óseas; 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; genetisk sjukdom; 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; malattia genetica; 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; 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; osteogenesis imperfecta; samoistna łamliwość kości; sostnienie niezupełne; choroba Vrolika; אוסטיאוגנסיס אימפרפקטה; אוסטאוגנסיס אימפרפקטה; Osteogenesis Imperfecta; אוסטאוגנזה אימפרפקטה; אוסטאוגנזיס אימפרפקטה; ଓଷ୍ଟିଓଜେନେସିସ ଇମ୍ପରଫେକ୍ଟା; 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; Sindrom Vrolik; Penyakit tulang rapuh; Sindrom Ekman-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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Instance of
  • designated intractable/rare disease
  • rare disease
  • class of disease
Subclass of
  • osteochondrodysplasia
  • disease
Authority file
Wikidata Q749409
BNCF Thesaurus ID:
NL CR AUT ID:
National Library of Spain SpMaBN ID (BNE v1.0):
National Library of Israel J9U ID:
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Subcategories

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

 

  • X-rays of osteogenesis imperfecta (4 C, 1 F)

B

  • Fredrick Brennan (2 C, 4 F)

E

  • Evianne van Gijn (1 F)

Media in category "Osteogenesis imperfecta"

The following 18 files are in this category, out of 18 total.

  • A-Missense-Mutation-in-the-SERPINH1-Gene-in-Dachshunds-with-Osteogenesis-Imperfecta-pgen.1000579.s007.ogv 29 s, 320 × 240; 2.84 MB
  • Characteristically blue sclerae of patient with osteogenesis imperfecta.jpg 970 × 453; 61 KB
  • Comparison of the designs of three different Fassier–Duval nails.png 2,000 × 1,196; 2.87 MB
  • ElizaSuggs.jpg 380 × 563; 34 KB
  • First appearance in print of «osteogenesis imperfecta» (header only).jpg 607 × 341; 46 KB
  • First appearance in print of «osteogenesis imperfecta».jpg 1,200 × 1,613; 528 KB
  • Hastings Gilford 11.jpg 602 × 1,181; 119 KB
  • Macro Fémur et Tibia - Ostéopsathyrose 55-o.apatho-852d-febia.jpg 379 × 1,648; 334 KB
  • Macro Fémur et Tibia - Ostéopsathyrose 55-o.apatho-852p-febia.jpg 686 × 1,496; 559 KB
  • Osteogenesis Imperfecta 1.jpg 495 × 684; 104 KB
  • Osteogenesis Imperfecta 2.jpg 611 × 897; 238 KB
  • Osteogenesis Imperfecta 3.jpg 613 × 904; 206 KB
  • Osteogenesis Imperfecta 4.jpg 615 × 894; 220 KB
  • Osteogenesis Imperfecta 5.jpg 608 × 893; 153 KB
  • Osteogenesis sclerae.gif 668 × 513; 294 KB
  • Tip of a Fassier–Duval intramedullary rod manufactured by Pega Medical.png 411 × 731; 350 KB
  • Two postoperative radiographs of a patient who underwent rodding surgery for osteogenesis imperfecta.png 2,000 × 2,000; 1.73 MB
  • Willem Vrolik's specimen of an infant with osteogenesis imperfecta.jpg 1,200 × 1,602; 1,001 KB
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