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DOID:0080117 - mitochondrial complex III deficiency nuclear type 8
Disease Ontology 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.
Synonyms:
Xenbase Genes : lyrm7
MONDO:0014364 - mitochondrial complex III deficiency nuclear type 8 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee