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G12.24 – Familial motor neuron disease
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G12.25 – Progressive spinal muscle atrophy
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G12.21 – Amyotrophic lateral sclerosis
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G11.4 – Hereditary spastic paraplegia
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G11.5 – Hypomyelination – hypogonadotropic hypogonadism – hypodontia
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G11.6 – Leukodystrophy with vanishing white matter disease
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G11.8 – Other hereditary ataxias
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G11.9 – Hereditary ataxia, unspecified
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G12.0 – Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
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G12.1 – Other inherited spinal muscular atrophy