Spastic Paraplegia 55, Autosomal Recessive
Combined Oxidative Phosphorylation Deficiency 7
Neuropathy, Hereditary Motor and Sensory, Type Via, with Optic Atrophy
Paraplegia
Neuropathy
Mitochondrial Disease
Combined Oxidative Phosphorylation Deficiency
Charcot-Marie-Tooth Disease, Axonal, Type 2e
3-Methylglutaconic Aciduria, Type Iii
Kearns-Sayre Syndrome