About   Help   FAQ
Disease Ontology Browser
molybdenum cofactor deficiency (DOID:0111165)
Alliance: disease page
Synonyms: combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase; MOCOD
Alt IDs: ICD10CM:E72.1, MESH:C535811, OMIM:PS252150, ORDO:99732
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.

Disease References using Mouse Models (4)
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory