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Metadata
ID	DOID:0080114
Name	mitochondrial complex III deficiency nuclear type 5
Definition	A mitochondrial complex III deficiency characterized by neonatal onset of severe metabolic acidosis associated with hyperammonemia and hypoglycemia and that has_material_basis_in homozygous mutation in the UQCRC2 gene on chromosome 16p12. http://omim.org/entry/615160?search=615160&highlight=615160
Xrefs	MIM:615160
Parent Relationships	is_a mitochondrial complex III deficiency
Subclass Logical Relationships	disease has basis in some structural_variant