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Disease Ontology Browser
molybdenum cofactor deficiency type A (DOID:0111164)
Alliance: disease page
Synonyms: combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type A; MOCOD type A; MOCODA; molybdenum cofactor deficiency complementation group A
Alt IDs: OMIM:252150, MESH:C565372, ORDO:308386, UMLS_CUI:C1854988
Definition: A molybdenum cofactor deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the MOCS1 gene on chromosome 6p21.

Disease References using Mouse Models (3)
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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04/09/2024
MGI 6.23 		The Jackson Laboratory