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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)
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12/10/2024
MGI 6.24 		The Jackson Laboratory