has material basis in germline mutation in GPHN sulfite oxidase deficiency due to molybdenum cofactor deficiency type C https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/molybdenum_cofactor_deficiency_type_c MOCODC molybdenum cofactor deficiency C UMLS:C1854990 molybdenum cofactor deficiency, complementation group type C DOID:0111166 MONDO:0014212 OMIM:615501 A molybdenum cofactor deficiency that has material basis in homozygous mutation in the GPHN gene on chromosome 14q23. combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type C Orphanet:308400 molybdenum cofactor deficiency type C MESH:C565374 molybdenum cofactor deficiency, complementation group C MEDGEN:340761 PMID:11095995 MOCOD type C GARD:0017388 sulfite oxidase deficiency due to molybdenum cofactor deficiency