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124528002: Deficiency of inosine monophosphate cyclohydrolase (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
204623013 Deficiency of IMP cyclohydrolase en Synonym Active Initial character case insensitive SNOMED CT core
2973100012 Deficiency of inosine monophosphate cyclohydrolase (disorder) en Fully specified name Active Case insensitive SNOMED CT core
2973234019 Deficiency of inosine monophosphate cyclohydrolase en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

REPLACED BY association reference set

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