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 C10 Nervous System Diseases D009422 +
  C10.574 Neurodegenerative Diseases D019636 +
   C10.574.500 Heredodegenerative Disorders, Nervous System D020271 +
     C10.574.500.362 Cockayne Syndrome D003057 
     C10.574.500.393 Dystonia Musculorum Deformans D004422 
     C10.574.500.850 Tourette Syndrome D005879 
     C10.574.500.487 Hallervorden-Spatz Syndrome D006211 
     C10.574.500.492 Hepatolenticular Degeneration D006527 
     C10.574.500.497 Huntington Disease D006816 
     C10.574.500.540 Menkes Kinky Hair Syndrome D007706 
     C10.574.500.536 Lesch-Nyhan Syndrome D007926 
     C10.574.500.542 Muscular Dystrophies D009136 +
     C10.574.500.547 Myotonic Dystrophy D009223 
     C10.574.500.545 Myotonia Congenita D009224 
     C10.574.500.550 Neuronal Ceroid-Lipofuscinosis D009472 
     C10.574.500.496 Hereditary Sensory and Autonomic Neuropathies D009477 +
     C10.574.500.825 Spinocerebellar Degenerations D013132 +
     C10.574.500.865 Tuberous Sclerosis D014402 
     C10.574.500.812 Spinal Muscular Atrophies of Childhood D014897 
     C10.574.500.495 Hereditary Motor and Sensory Neuropathies D015417 +
     C10.574.500.662 Optic Atrophies, Hereditary D015418 +
     C10.574.500.775 Rett Syndrome D015518 
     C10.574.500.425 Gerstmann-Straussler-Scheinker Disease D016098 
     C10.574.500.549 Neurofibromatoses D017253 +
     C10.574.500.300 Canavan Disease D017825 
     C10.574.500.529 Lafora Disease D020192 
     C10.574.500.875 Unverricht-Lundborg Syndrome D020194 
     C10.574.500.494 Hereditary Central Nervous System Demyelinating Diseases D020279 
     C10.574.500.050 Amyloid Neuropathies, Familial D028227 
     C10.574.500.024 Alexander Disease D038261 

 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
  C16.320 Genetic Diseases, Inborn D030342 +
   C16.320.400 Heredodegenerative Disorders, Nervous System D020271 +
     C16.320.400.200 Cockayne Syndrome D003057 
     C16.320.400.330 Dystonia Musculorum Deformans D004422 
     C16.320.400.820 Tourette Syndrome D005879 
     C16.320.400.375 Hallervorden-Spatz Syndrome D006211 
     C16.320.400.387 Hepatolenticular Degeneration D006527 
     C16.320.400.430 Huntington Disease D006816 
     C16.320.400.520 Menkes Kinky Hair Syndrome D007706 
     C16.320.400.500 Lesch-Nyhan Syndrome D007926 
     C16.320.400.530 Muscular Dystrophies D009136 +
     C16.320.400.542 Myotonic Dystrophy D009223 
     C16.320.400.540 Myotonia Congenita D009224 
     C16.320.400.600 Neuronal Ceroid-Lipofuscinosis D009472 
     C16.320.400.415 Hereditary Sensory and Autonomic Neuropathies D009477 +
     C16.320.400.780 Spinocerebellar Degenerations D013132 +
     C16.320.400.880 Tuberous Sclerosis D014402 
     C16.320.400.765 Spinal Muscular Atrophies of Childhood D014897 
     C16.320.400.400 Hereditary Motor and Sensory Neuropathies D015417 +
     C16.320.400.630 Optic Atrophies, Hereditary D015418 +
     C16.320.400.700 Rett Syndrome D015518 
     C16.320.400.350 Gerstmann-Straussler-Scheinker Disease D016098 
     C16.320.400.560 Neurofibromatoses D017253 +
     C16.320.400.150 Canavan Disease D017825 
     C16.320.400.480 Lafora Disease D020192 
     C16.320.400.940 Unverricht-Lundborg Syndrome D020194 
     C16.320.400.393 Hereditary Central Nervous System Demyelinating Diseases D020279 
     C16.320.400.050 Amyloid Neuropathies, Familial D028227 
     C16.320.400.024 Alexander Disease D038261 
     C16.320.400.525 Mental Retardation, X-Linked D038901 +