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237945003: Complete deficiency of methylmalonyl-coenzyme A mutase (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
356623016 Mutase0 methylmalonic acidemia en Synonym Active Entire term case insensitive SNOMED CT core module
356624010 Complete deficiency of methylmalonyl-CoA mutase en Synonym Active Only initial character case insensitive SNOMED CT core module
356625011 Mutase0 methylmalonic acidaemia en Synonym Active Entire term case insensitive SNOMED CT core module
2971387014 Complete deficiency of methylmalonyl-coenzyme A mutase (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
2971787011 Complete deficiency of methylmalonyl-coenzyme A mutase en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Complete deficiency of methylmalonyl-coenzyme A mutase Is a Methylmalonyl-CoA mutase deficiency false Inferred relationship Existential restriction modifier
Complete deficiency of methylmalonyl-coenzyme A mutase Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Complete deficiency of methylmalonyl-coenzyme A mutase Finding site Body system structure false Inferred relationship Existential restriction modifier
Complete deficiency of methylmalonyl-coenzyme A mutase Is a Deficiency of methylmalonyl-coenzyme A mutase true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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