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124244005: Deficiency of phosphoribosylglycinamide formyltransferase (disorder)

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
203830013 Deficiency of phosphoribosylglycinamide formyltransferase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
727784018 Deficiency of phosphoribosylglycinamide formyltransferase (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
203830013 Deficiency of phosphoribosylglycinamide formyltransferase en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
203830013 Deficiency of phosphoribosylglycinamide formyltransferase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
727784018 Deficiency of phosphoribosylglycinamide formyltransferase (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
727784018 Deficiency of phosphoribosylglycinamide formyltransferase (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4770921000241110 déficit en phosphoribosyl-glycinamide formyltransférase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4770921000241110 déficit en phosphoribosyl-glycinamide formyltransférase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deficiency of phosphoribosylglycinamide formyltransferase (disorder) Is a Deficiency of transferase true Inferred relationship Existential restriction modifier (core metadata concept)
Deficiency of phosphoribosylglycinamide formyltransferase (disorder) Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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