• Charcot-Marie-Tooth Disease, axonal, type 2GG
  Charcot-Marie-Tooth Disease, axonal, type 2GG
  MedGen
• Basal ganglia calcification, idiopathic, 8, autosomal recessive
  Basal ganglia calcification, idiopathic, 8, autosomal recessive
  MedGen
• Cataract, ataxia, short stature, and intellectual disability
  Cataract, ataxia, short stature, and intellectual disability
  MedGen
• Hereditary spastic paraplegia 15
  Hereditary spastic paraplegia 15
  MedGen
• Hypomyelinating leukodystrophy 9
  Hypomyelinating leukodystrophy 9
  MedGen

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