Misplaced Pages

The following pages link to Neurofibromatosis type II

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• Charcot–Marie–Tooth disease (links | edit)
• Von Hippel–Lindau disease (links | edit)
• Joubert syndrome (links | edit)
• Neurofibromatosis (links | edit)
• List of genetic disorders (links | edit)
• NF2 (links | edit)
• Megalencephaly (links | edit)
• Wolff–Parkinson–White syndrome (links | edit)
• 1822 in science (links | edit)
• Proteus syndrome (links | edit)
• Cardiofaciocutaneous syndrome (links | edit)
• Tuberous sclerosis (links | edit)
• Neurofibromatosis Type 2 (redirect page) (links | edit)
  • Glossary of communication disorders (links | edit)
  • ThriftyComputer (links | edit)
  • User talk:Bluemoose/archive3 (links | edit)
  • User talk:Davidruben/Archive 1 (links | edit)
• Noonan syndrome (links | edit)
• Vestibular schwannoma (links | edit)
• Li–Fraumeni syndrome (links | edit)
• Spinal tumor (links | edit)
• Ependymoma (links | edit)
• Ataxia–telangiectasia (links | edit)
• Peutz–Jeghers syndrome (links | edit)
• Incontinentia pigmenti (links | edit)
• CADASIL (links | edit)
• Coffin–Lowry syndrome (links | edit)
• Neurofibromatosis type I (links | edit)
• Bardet–Biedl syndrome (links | edit)
• Hamartoma (links | edit)
• X-linked agammaglobulinemia (links | edit)
• Sturge–Weber syndrome (links | edit)
• Cowden syndrome (links | edit)
• Cherubism (links | edit)
• Carpenter syndrome (links | edit)
• Metachondromatosis (links | edit)
• Abdallat–Davis–Farrage syndrome (links | edit)
• Phakomatosis (links | edit)
• Angiomatosis (links | edit)
• McCune–Albright syndrome (links | edit)
• Neurofibromatosis type 2 (redirect page) (links | edit)
  • Genetic disorder (links | edit)
  • Hearing loss (links | edit)
  • Neurofibromatosis (links | edit)
  • List of diseases (N) (links | edit)
  • Cataract (links | edit)
  • Lisch nodule (links | edit)
  • Meningioma (links | edit)
  • Index of oncology articles (links | edit)
  • Chromosome 22 (links | edit)
  • Cerebellopontine angle syndrome (links | edit)
  • List of abbreviations for diseases and disorders (links | edit)
  • List of OMIM disorder codes (links | edit)
  • List of genes mutated in cutaneous conditions (links | edit)
  • James F. Gusella (links | edit)
  • Causes of hearing loss (links | edit)
  • Talk:Neurofibromatosis/Archive 1 (links | edit)
  • User:Davidruben/OrphaNet (links | edit)
  • User:Sbakerrrrr01/sandbox (links | edit)
  • User:Y-S.Ko/Wikipedia course2/Internal Medicine (links | edit)
  • User talk:Anandks007/Med (links | edit)
  • Misplaced Pages:WikiProject Medicine/Dermatology task force/Missing articles/LeBoit (links | edit)
• Optic nerve sheath meningioma (links | edit)
• Costello syndrome (links | edit)
• ZAP70 deficiency (links | edit)
• List of ICD-9 codes 740–759: congenital anomalies (links | edit)
• Carney complex (links | edit)
• Bannayan–Riley–Ruvalcaba syndrome (links | edit)
• Merlin (protein) (links | edit)
• Seckel syndrome (links | edit)
• MISME Syndrome (redirect page) (links | edit)
  • Misme (links | edit)
• Schwannomatosis (links | edit)
• Neurofibromatosis II (redirect page) (links | edit)
  • User:Rich Farmbrough/temp68 (links | edit)
  • Misplaced Pages talk:WikiProject Medicine/Dermatology task force/Missing articles/Archive 1 (links | edit)
• Pallister–Hall syndrome (links | edit)
• Neurofibromatosis 2 (redirect page) (links | edit)
  • Meningioma (links | edit)
  • List of MeSH codes (C16) (links | edit)
  • List of MeSH codes (C10) (links | edit)
  • List of MeSH codes (C09) (links | edit)
  • List of MeSH codes (C04) (links | edit)
  • User:DerekvG/sandbox/braintumor/meningioma (links | edit)
  • User:HeorteTheCenre/sandbox (links | edit)
  • User:Brainist/MeSH articles (links | edit)