Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1

Parents (7)

• 85995004Autosomal recessive hereditary disorder disorder
• 66091009Congenital disease disorder
• 363080007Digestive system hereditary disorder disorder
• 42357009Disorder of digestive system specific to fetus OR newborn disorder
• 13920009Hepatic encephalopathy disorder
• 363235000Hereditary disorder of nervous system disorder
• 235903001Metabolic and genetic disorder affecting the liver disorder

Children (0)

None (leaf concept).