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DOID:0111164 - molybdenum cofactor deficiency type A
Disease Ontology Definition:A molybdenum cofactor deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the MOCS1 gene on chromosome 6p21.
Synonyms: MOCOD type A, MOCODA, combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type A, molybdenum cofactor deficiency complementation group A,
Echinobase Genes : mocs1
MIM:252150 - molybdenum cofactor deficiency, complementation group a; mocoda |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
molybdenum cofactor deficiency (is_a)