Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
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 Disease Ontology (on Monarch Initiative):
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
Parent(s): genetic disease (is_a), mitochondrial complex III deficiency (is_a)