29692004: Combined molybdoflavoprotein enzyme deficiency (disorder)

SNOMED CT Concept\constatation clinique\Disease\...

\Genetic disease\maladie héréditaire\xanthinurie héréditaire (trouble)\Combined molybdoflavoprotein enzyme deficiency

\trouble métabolique\Disorder of purine and pyrimidine metabolism\troubles du métabolisme des purines\xanthinurie héréditaire (trouble)\Combined molybdoflavoprotein enzyme deficiency
\trouble métabolique\Enzymopathy\xanthinurie héréditaire (trouble)\Combined molybdoflavoprotein enzyme deficiency

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

484364013 Hereditary xanthinuria type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
484365014 Molybdenum cofactor deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
484366010 Combined xanthine oxidase and aldehyde oxidase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
484367018 Xanthine oxidase-sulphite oxidase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
484368011 Combined xanthine oxidase and sulfite oxidase and aldehyde oxidase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
484369015 Combined xanthine oxidase and sulphite oxidase and aldehyde oxidase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
49668019 Combined molybdoflavoprotein enzyme deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
49669010 Hereditary xanthinuria, type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
49670011 Deficiency of molybdenum cofactor en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
49671010 Xanthine oxidase-sulfite oxidase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
760614019 Combined molybdoflavoprotein enzyme deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Combined molybdoflavoprotein enzyme deficiency	est un(e) (attribut)	xanthinurie héréditaire (trouble)	true	Inferred relationship	Some
Combined molybdoflavoprotein enzyme deficiency	survenue (attribut)	congénital	false	Inferred relationship	Some
Combined molybdoflavoprotein enzyme deficiency	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Molybdenum cofactor deficiency complementation group C	est un(e) (attribut)	True	Combined molybdoflavoprotein enzyme deficiency	Inferred relationship	Some
Molybdenum cofactor deficiency complementation group A	est un(e) (attribut)	True	Combined molybdoflavoprotein enzyme deficiency	Inferred relationship	Some
Molybdenum cofactor deficiency complementation group B	est un(e) (attribut)	True	Combined molybdoflavoprotein enzyme deficiency	Inferred relationship	Some

This concept is not in any reference sets