CPT Changes
Current book and archives back to 2000 Easy-to-read online book format Linked to and from code details
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Combined molybdoflavoprotein enzyme deficiency 29692004 SNOMED CT code SNOMED code 29692004 name Combined molybdoflavoprotein enzyme deficiency status active date introduced 2002-01-31 fully specified name(s) Combined molybdoflavoprotein enzyme deficiency (disorder) synonyms Hereditary xanthinuria type 2 Molybdenum cofactor deficiency Combined xanthine oxidase and aldehyde oxidase deficiency Xanthine oxidase-sulphite oxidase deficiency Combined xanthine oxidase and sulfite oxidase and aldehyde oxidase deficiency Combined xanthine oxidase and sulphite oxidase and aldehyde oxidase deficiency Combined molybdoflavoprotein enzyme deficiency Hereditary xanthinuria, type 2 Deficiency of molybdenum cofactor Xanthine oxidase-sulfite oxidase deficiency attributes - group1 Finding site Kidney structure 64033007 parents Hereditary xanthinuria 54627004 children Molybdenum cofactor deficiency complementation group A 1003367004 Molybdenum cofactor deficiency complementation group B 1003368009 Molybdenum cofactor deficiency complementation group C 1003387003 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Hereditary metabolic disease 1821000146108 Hereditary xanthinuria 54627004 Combined molybdoflavoprotein enzyme deficiency 29692004 ancestors sorted most to least specific
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