All
 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