Kjer's optic neuropathy||208.16 Dentatorubral-pallidoluysian atrophy||136.1 SMN1||128.1 Optic atrophy 1||104.08 ATN1||104.08 Socialized Hate||104.08 Muscle atrophy||104.08 Optic atrophy||96.07 Spinal muscular atrophy||96.07 List of diseases (O)||88.07 Amyotrophic lateral sclerosis||80.06 Parry-Romberg syndrome||80.06 Violent by Nature||80.06 Motor neurone disease||80.06 Muscle||72.05 Cellular adaptation||72.05 Kugelberg-Welander disease||64.05 Progressive retinal atrophy||64.05 FBXO32||64.05 List of diseases (S)||64.05 OPA3||56.04 Cerebral atrophy||56.04 Metal Forces||48.03 Survival of motor neuron protein-interacting protein 1||48.03 Kennedy disease||48.03 Multiple system atrophy||48.03 Frontotemporal dementia||48.03 Werdnig-Hoffman disease||48.03 Atrophic vaginitis||48.03 Spinal Muscular Atrophy Type 2||48.03 NAIP||40.03 Hereditary Neuralgic Amyotrophy||40.03 Semantic dementia||40.03 Exocrine pancreatic insufficiency||40.03 Leber's hereditary optic neuropathy||40.03 Spinocerebellar ataxia||40.03 IGHMBP2||32.02 Microvillous inclusion disease||32.02 HSPB8||32.02 List of neurological disorders||32.02 Olivopontocerebellar atrophy||32.02 Dermatomyositis||32.02 Astemizole||24.01 Progressive muscular atrophy||24.01 Cone dystrophy||24.01 Shy-Drager syndrome||24.01 Anterior horn (spinal cord)||24.01 Wolfram syndrome||24.01