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DOID:0111165 - molybdenum cofactor deficiency
Disease Ontology Definition:A metal metabolism disease characterized by encephalopathy that worsens over time resulting from the absence of molybdenum cofactor which leads to accumulation of toxic levels of sulphite and neurological damage.
Synonyms: MOCOD, combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase,
Xenbase Genes
:
mocs2,
gphn,
mocs1
| MONDO:0020480 - sulfite oxidase deficiency due to molybdenum cofactor deficiency |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
metal metabolism disorder (is_a)