Misplaced Pages

The following pages link to Weissenbacher–Zweymüller syndrome

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Showing 50 items.

• Genetic disorder (links | edit)
• List of genetic disorders (links | edit)
• Ehlers–Danlos syndrome (links | edit)
• Alport syndrome (links | edit)
• Osteogenesis imperfecta (links | edit)
• Goodpasture syndrome (links | edit)
• Weissenbacher Zweymuller syndrome (redirect page) (links | edit)
  • User talk:Anandks007/Med (links | edit)
• Stickler syndrome (links | edit)
• Fuchs' dystrophy (links | edit)
• Weissenbacher-Zweymuller syndrome (redirect page) (links | edit)
  • Collagen, type XI, alpha 2 (links | edit)
• Spondyloperipheral dysplasia (links | edit)
• Collagenopathy, types II and XI (links | edit)
• Hypochondrogenesis (links | edit)
• Achondrogenesis type 2 (links | edit)
• Kniest dysplasia (links | edit)
• Otospondylomegaepiphyseal dysplasia (links | edit)
• Spondyloepiphyseal dysplasia congenita (links | edit)
• Spondyloepimetaphyseal dysplasia, Strudwick type (links | edit)
• Bullous pemphigoid (links | edit)
• Nonsyndromic deafness (links | edit)
• Platyspondylic lethal skeletal dysplasia, Torrance type (links | edit)
• Infantile cortical hyperostosis (links | edit)
• Pierre Robin sequence (links | edit)
• WZS (redirect page) (links | edit)
  • User:Brycehughes/pad2 (links | edit)
  • User:BD2412/TLA (links | edit)
  • Misplaced Pages:TLAs from UAA to XZZ (links | edit)
• Sack–Barabas syndrome (links | edit)
• Multiple epiphyseal dysplasia (links | edit)
• Pseudoachondroplasia (links | edit)
• Raine syndrome (links | edit)
• Dermatopathia pigmentosa reticularis (links | edit)
• Pachyonychia congenita (links | edit)
• Bethlem myopathy (links | edit)
• Epidermolysis bullosa dystrophica (links | edit)
• Collagen disease (links | edit)
• Weissenbacher-Zweymueller syndrome (redirect page) (links | edit)
• Urbach–Wiethe disease (links | edit)
• Marshall syndrome (links | edit)
• Bart syndrome (links | edit)
• Metaphyseal chondrodysplasia Schmid type (links | edit)
• Junctional epidermolysis bullosa (medicine) (links | edit)
• Transient bullous dermolysis of the newborn (links | edit)
• Ullrich congenital muscular dystrophy (links | edit)
• Collagen VI (links | edit)
• Congenital stromal corneal dystrophy (links | edit)
• Laryngo-onycho-cutaneous syndrome (links | edit)
• List of OMIM disorder codes (links | edit)
• Weissenbacher-Zweymüller syndrome (redirect page) (links | edit)
  • Collagenopathy, types II and XI (links | edit)
  • Otospondylomegaepiphyseal dysplasia (links | edit)
  • Collagen, type XI, alpha 2 (links | edit)
  • User:Jfdwolff/Braglist (links | edit)
  • User:Jfdwolff (links | edit)
  • Misplaced Pages:WikiProject Medicine/Medical genetics task force/Open Tasks (links | edit)
• Weissenbacher–Zweymuller syndrome (redirect page) (links | edit)
  • List of diseases (W) (links | edit)
• Knobloch syndrome (links | edit)
• List of syndromes (links | edit)
• Pierre Robin syndrome fetal chondrodysplasia (redirect page) (links | edit)
  • User talk:Anandks007/Med (links | edit)