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C10 Nervous System Diseases D009422 +
C10.597 Neurologic Manifestations D009461 +
C10.597.606 Neurobehavioral Manifestations D019954 +
C10.597.606.643 Mental Retardation D008607 +
C10.597.606.643.455 Mental Retardation, X-Linked D038901 +
C10.597.606.643.455.124 Adrenoleukodystrophy D000326
C10.597.606.643.455.500 Fragile X Syndrome D005600
C10.597.606.643.455.687 Menkes Kinky Hair Syndrome D007706
C10.597.606.643.455.625 Lesch-Nyhan Syndrome D007926
C10.597.606.643.455.875 Pyruvate Dehydrogenase Complex Deficiency Disease D015325
C10.597.606.643.455.937 Rett Syndrome D015518
C10.597.606.643.455.750 Mucopolysaccharidosis II D016532
C10.597.606.643.455.249 Coffin-Lowry Syndrome D038921
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
C16.320 Genetic Diseases, Inborn D030342 +
C16.320.322 Genetic Diseases, X-Linked D040181 +
C16.320.322.500 Mental Retardation, X-Linked D038901 +
C16.320.322.500.124 Adrenoleukodystrophy D000326
C16.320.322.500.500 Fragile X Syndrome D005600
C16.320.322.500.687 Menkes Kinky Hair Syndrome D007706
C16.320.322.500.625 Lesch-Nyhan Syndrome D007926
C16.320.322.500.875 Pyruvate Dehydrogenase Complex Deficiency Disease D015325
C16.320.322.500.937 Rett Syndrome D015518
C16.320.322.500.750 Mucopolysaccharidosis II D016532
C16.320.322.500.249 Coffin-Lowry Syndrome D038921
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
C16.320 Genetic Diseases, Inborn D030342 +
C16.320.400 Heredodegenerative Disorders, Nervous System D020271 +
C16.320.400.525 Mental Retardation, X-Linked D038901 +
C16.320.400.525.124 Adrenoleukodystrophy D000326
C16.320.400.525.500 Fragile X Syndrome D005600
C16.320.400.525.687 Menkes Kinky Hair Syndrome D007706
C16.320.400.525.625 Lesch-Nyhan Syndrome D007926
C16.320.400.525.875 Pyruvate Dehydrogenase Complex Deficiency Disease D015325
C16.320.400.525.937 Rett Syndrome D015518
C16.320.400.525.750 Mucopolysaccharidosis II D016532
C16.320.400.525.249 Coffin-Lowry Syndrome D038921
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