Term Name:	molybdenum cofactor deficiency type B
Synonyms:	combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type B, MOCOD type B, MOCODB, molybdenum cofactor deficiency complementation group B
Definition:	A molybdenum cofactor deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the MOCS2 gene on chromosome 5q11.
Ontology:	Human Disease [DOID:0111163]   ( DOID:0111163 )