Term Name:	mitochondrial complex III deficiency nuclear type 8
Synonyms:
Definition:	A mitochondrial complex III deficiency characterized by childhood onset of progressive neurodegeneration that has_material_basis_in homozygous mutation in the LYRM7 gene on chromosome 5q23.
Ontology:	Human Disease [DOID:0080117]   ( DOID:0080117 )