Search Ontology:
Human Disease
molybdenum cofactor deficiency
- Term ID
- DOID:0111165
- Synonyms
-
- combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase
- MOCOD
- 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. (3)
- References
-
- GARD:3705
- ICD10CM:E72.1
- MESH:C535811
- MIM:PS252150
- ORDO:99732
- Ontology
- Human Disease ( DOID:0111165 )
- is a type of
-
- has subtype
-
Other Pages
Genes Involved
Zebrafish Models