About   Help   FAQ
Disease Ontology Browser
molybdenum cofactor deficiency type B (DOID:0111163)
Alliance: disease page
Synonyms: combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type B; MOCOD type B; MOCODB; molybdenum cofactor deficiency complementation group B
Alt IDs: OMIM:252160, MESH:C565373, ORDO:308393, UMLS_CUI:C1854989
Definition: A molybdenum cofactor deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the MOCS2 gene on chromosome 5q11.

Disease References using Mouse Models (1)
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