Misplaced Pages

The following pages link to Glanzmann's thrombasthenia

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Showing 50 items.

• Apert syndrome (links | edit)
• Thanatophoric dysplasia (links | edit)
• Evans syndrome (links | edit)
• Hematocele (links | edit)
• Coagulopathy (links | edit)
• Hemothorax (links | edit)
• Glanzmann thrombasthenia (redirect page) (links | edit)
  • List of diseases (G) (links | edit)
  • Plateletpheresis (links | edit)
  • Hemothorax (links | edit)
  • List of human clusters of differentiation (links | edit)
  • Bernard–Soulier syndrome (links | edit)
  • User:Synonymous-solecism/Coagulopathy (links | edit)
  • User talk:Anandks007/Med (links | edit)
• Glanzmann disease (redirect page) (links | edit)
• Leber congenital amaurosis (links | edit)
• Leukocyte adhesion deficiency (links | edit)
• Hypogammaglobulinemia (links | edit)
• Hyphema (links | edit)
• Hypochondroplasia (links | edit)
• Glanzmann's disease (redirect page) (links | edit)
• Common variable immunodeficiency (links | edit)
• Erik Adolf von Willebrand (links | edit)
• ABCD syndrome (links | edit)
• Renal vein thrombosis (links | edit)
• Congenital afibrinogenemia (links | edit)
• Hypoprothrombinemia (links | edit)
• Jackson–Weiss syndrome (links | edit)
• Pfeiffer syndrome (links | edit)
• Hermansky–Pudlak syndrome (links | edit)
• Nephrogenic diabetes insipidus (links | edit)
• Hemarthrosis (links | edit)
• Pseudohypoparathyroidism (links | edit)
• Bernard–Soulier syndrome (links | edit)
• Activated protein C resistance (links | edit)
• Familial male-limited precocious puberty (links | edit)
• List of ICD-9 codes 280–289: diseases of the blood and blood-forming organs (links | edit)
• Thrombocytopenic purpura (links | edit)
• Glycoprotein IIb/IIIa inhibitors (links | edit)
• Glycoprotein IIb/IIIa (links | edit)
• Thrombasthenia (redirect page) (links | edit)
  • List of diseases (T) (links | edit)
  • Basset Hound (links | edit)
  • List of MeSH codes (C16) (links | edit)
  • List of MeSH codes (C15) (links | edit)
  • Clot retraction (links | edit)
  • User:Brainist/MeSH articles (links | edit)
  • User talk:Anandks007/Med (links | edit)
• Protein C deficiency (links | edit)
• Factor X deficiency (links | edit)
• Factor VII deficiency (links | edit)
• Factor XIII deficiency (links | edit)
• Ristocetin (links | edit)
• X-linked severe combined immunodeficiency (links | edit)
• Selective immunoglobulin A deficiency (links | edit)
• Nevoid basal-cell carcinoma syndrome (links | edit)
• Piebaldism (links | edit)
• Robinow syndrome (links | edit)
• XX gonadal dysgenesis (links | edit)
• TNF receptor associated periodic syndrome (links | edit)
• Loeys–Dietz syndrome (links | edit)
• Hemoperitoneum (links | edit)
• Hypohidrotic ectodermal dysplasia (links | edit)
• Familial hypercholesterolemia (links | edit)