mitochondrial complex III deficiency nuclear type 8 Disease Ontology Browser

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Disease Ontology Browser

mitochondrial complex III deficiency nuclear type 8 (DOID:0080117)
Alliance: disease page
Alt IDs: OMIM:615838
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.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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