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DOID:0111163 - molybdenum cofactor deficiency type B
Disease Ontology Definition:A molybdenum cofactor deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the MOCS2 gene on chromosome 5q11.
Synonyms: MOCOD type B, MOCODB, combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type B, molybdenum cofactor deficiency complementation group B,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0009644 - sulfite oxidase deficiency due to molybdenum cofactor deficiency type B |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee