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238011005: Inosine triphosphate pyrophosphohydrolase deficiency (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
356742011 Inosine triphosphate pyrophosphohydrolase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
356743018 ITPase - Inosine triphosphatase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
626829012 Inosine triphosphate pyrophosphohydrolase deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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