Combined oxidative phosphorylation defect type 39

Parents (6)

• 85995004Autosomal recessive hereditary disorder disorder
• 363070008Developmental hereditary disorder disorder
• 1362108000Genetic intellectual disability disorder
• 363212003Hereditary disorder of musculoskeletal system disorder
• 16851005Mitochondrial myopathy disorder
• 1137472008Neurodevelopmental delay disorder

Children (0)

None (leaf concept).