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238011005: Inosine triphosphate pyrophosphohydrolase deficiency (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
356742011 Inosine triphosphate pyrophosphohydrolase deficiency en Synonym Active Case insensitive SNOMED CT core
356743018 ITPase - Inosine triphosphatase deficiency en Synonym Active Case sensitive SNOMED CT core
626829012 Inosine triphosphate pyrophosphohydrolase deficiency (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Inosine triphosphate pyrophosphohydrolase deficiency Finding site Body system structure false Inferred relationship Some
Inosine triphosphate pyrophosphohydrolase deficiency Occurrence Congenital false Inferred relationship Some
Inosine triphosphate pyrophosphohydrolase deficiency Is a Disorder of purine metabolism true 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

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