124528002: Deficiency of inosine monophosphate cyclohydrolase (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\Metabolic disease\Enzymopathy\Specific enzyme deficiency\Deficiency of inosine monophosphate cyclohydrolase (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

204623013 Deficiency of IMP cyclohydrolase en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2973100012 Deficiency of inosine monophosphate cyclohydrolase (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2973234019 Deficiency of inosine monophosphate cyclohydrolase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

7162681000241110 déficit en IMP cyclohydrolase fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Deficiency of inosine monophosphate cyclohydrolase (disorder)	Is a	Specific enzyme deficiency	true	Inferred relationship	Some
Deficiency of inosine monophosphate cyclohydrolase (disorder)	Finding site	Body system structure	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets