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860858001: Glycogen storage disease due to muscle pyruvate kinase deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2020. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3944365014 Glycogen storage disease due to muscle pyruvate kinase deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3944366010 Glycogen storage disease due to muscle pyruvate kinase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Glycogen storage disease due to muscle pyruvate kinase deficiency Is a Glycogen storage disease true Inferred relationship Existential restriction modifier
Glycogen storage disease due to muscle pyruvate kinase deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Glycogen storage disease due to muscle pyruvate kinase deficiency Due to Deficiency of pyruvate kinase true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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