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Summary Literature (0)
MIM:615501 - MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C; MOCODC

Xenbase Genes: gphn

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014212 - sulfite oxidase deficiency due to molybdenum cofactor deficiency type C
MONDO:0019358 - encephalopathy due to sulfite oxidase deficiency
MONDO:0020480 - sulfite oxidase deficiency due to molybdenum cofactor deficiency

Disease Ontology (DO):
DOID:0111166 - molybdenum cofactor deficiency type C