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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 +