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C10 Nervous System Diseases D009422 + C10.292 Cranial Nerve Diseases D003389 + C10.292.700 Optic Nerve Diseases D009901 + C10.292.700.225 Optic Atrophy D009896 + C10.292.700.225.500 Optic Atrophies, Hereditary D015418 + C10.292.700.225.500.980 Wolfram Syndrome D014929 C10.292.700.225.500.500 Optic Atrophy, Autosomal Dominant D029241 C10.292.700.225.500.400 Optic Atrophy, Hereditary, Leber D029242
C10 Nervous System Diseases D009422 + C10.574 Neurodegenerative Diseases D019636 + C10.574.500 Heredodegenerative Disorders, Nervous System D020271 + C10.574.500.662 Optic Atrophies, Hereditary D015418 + C10.574.500.662.980 Wolfram Syndrome D014929 C10.574.500.662.500 Optic Atrophy, Autosomal Dominant D029241 C10.574.500.662.400 Optic Atrophy, Hereditary, Leber D029242
C11 Eye Diseases D005128 + C11.270 Eye Diseases, Hereditary D015785 + C11.270.564 Optic Atrophies, Hereditary D015418 + C11.270.564.980 Wolfram Syndrome D014929 C11.270.564.500 Optic Atrophy, Autosomal Dominant D029241 C11.270.564.400 Optic Atrophy, Hereditary, Leber D029242
C11 Eye Diseases D005128 + C11.640 Optic Nerve Diseases D009901 + C11.640.451 Optic Atrophy D009896 + C11.640.451.451 Optic Atrophies, Hereditary D015418 + C11.640.451.451.980 Wolfram Syndrome D014929 C11.640.451.451.500 Optic Atrophy, Autosomal Dominant D029241 C11.640.451.451.400 Optic Atrophy, Hereditary, Leber D029242
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 + C16.320 Genetic Diseases, Inborn D030342 + C16.320.290 Eye Diseases, Hereditary D015785 + C16.320.290.564 Optic Atrophies, Hereditary D015418 + C16.320.290.564.980 Wolfram Syndrome D014929 C16.320.290.564.500 Optic Atrophy, Autosomal Dominant D029241 C16.320.290.564.400 Optic Atrophy, Hereditary, Leber D029242
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 + C16.320 Genetic Diseases, Inborn D030342 + C16.320.400 Heredodegenerative Disorders, Nervous System D020271 + C16.320.400.630 Optic Atrophies, Hereditary D015418 + C16.320.400.630.980 Wolfram Syndrome D014929 C16.320.400.630.500 Optic Atrophy, Autosomal Dominant D029241 C16.320.400.630.400 Optic Atrophy, Hereditary, Leber D029242