AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE
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(OMIM:205100)
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Autosomal dominant Charcot-Marie-Tooth disease type 2C
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(Orphanet:99937)
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Autosomal dominant spastic paraplegia type 10
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(Orphanet:100991)
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Autosomal recessive spastic paraplegia type 11
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(Orphanet:2822)
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BROWN-VIALETTO-VAN LAERE SYNDROME 1
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(OMIM:211530)
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Juvenile amyotrophic lateral sclerosis
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(Orphanet:300605)
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NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB
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(OMIM:607641)
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Neurodegeneration with brain iron accumulation due to C19orf12 mutation
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(Orphanet:289560)
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Riboflavin transporter deficiency
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(Orphanet:97229)
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SPINAL MUSCULAR ATROPHY, SEGMENTAL
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(OMIM:183020)
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Spondyloepiphyseal dysplasia, Reardon type
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(Orphanet:163662)
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