All

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 C10 Nervous System Diseases D009422 +
  C10.562 Neurocutaneous Syndromes D020752 
    C10.562.100 Ataxia Telangiectasia D001260 
    C10.562.400 Hippel-Lindau Disease D006623 
    C10.562.800 Sturge-Weber Syndrome D013341 
    C10.562.850 Tuberous Sclerosis D014402 
    C10.562.600 Neurofibromatoses D017253 +
 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
  C16.131 Abnormalities D000013 +
   C16.131.077 Abnormalities, Multiple D000015 +
    C16.131.077.350 Ectodermal Dysplasia D004476 +
     C16.131.077.350.712 Neurocutaneous Syndromes D020752 
 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
  C16.131 Abnormalities D000013 +
   C16.131.831 Skin Abnormalities D012868 +
    C16.131.831.350 Ectodermal Dysplasia D004476 +
     C16.131.831.350.712 Neurocutaneous Syndromes D020752 
 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
  C16.320 Genetic Diseases, Inborn D030342 +
   C16.320.850 Skin Diseases, Genetic D012873 +
    C16.320.850.250 Ectodermal Dysplasia D004476 +
     C16.320.850.250.712 Neurocutaneous Syndromes D020752 
 C17 Skin and Connective Tissue Diseases D017437 +
  C17.800 Skin Diseases D012871 +
   C17.800.804 Skin Abnormalities D012868 +
    C17.800.804.350 Ectodermal Dysplasia D004476 +
     C17.800.804.350.712 Neurocutaneous Syndromes D020752 
 C17 Skin and Connective Tissue Diseases D017437 +
  C17.800 Skin Diseases D012871 +
   C17.800.827 Skin Diseases, Genetic D012873 +
    C17.800.827.250 Ectodermal Dysplasia D004476 +
     C17.800.827.250.712 Neurocutaneous Syndromes D020752