1003368009: Molybdenum cofactor deficiency complementation group B (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Hereditary xanthinuria\Combined molybdoflavoprotein enzyme deficiency\Molybdenum cofactor deficiency complementation group B
• \Metabolic disease\Hereditary metabolic disease\Hereditary xanthinuria\Combined molybdoflavoprotein enzyme deficiency\Molybdenum cofactor deficiency complementation group B
• \Metabolic disease\Purine and pyrimidine metabolism disorder\Disorder of purine metabolism\Hereditary xanthinuria\Combined molybdoflavoprotein enzyme deficiency\Molybdenum cofactor deficiency complementation group B
• \Metabolic disease\Enzymopathy\Hereditary xanthinuria\Combined molybdoflavoprotein enzyme deficiency\Molybdenum cofactor deficiency complementation group B

Status: current, Primitive. Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4168093015	Molybdenum cofactor deficiency complementation group B	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
4168094014	Molybdenum cofactor deficiency complementation group B (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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