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40951006: Primary hyperoxaluria, type II (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
68304013 Primary hyperoxaluria, type II en Synonym Active Only initial character case insensitive SNOMED CT core module
68305014 Glyoxylate reductase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
68306010 Glyceric dehydrogenase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
68307018 L-glyceric aciduria en Synonym Active Entire term case sensitive SNOMED CT core module
68308011 Glycerate dehydrogenase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
492842013 Deficiency of glyoxylate reductase en Synonym Active Entire term case insensitive SNOMED CT core module
492843015 Deficiency of glycerate dehydrogenase en Synonym Active Entire term case insensitive SNOMED CT core module
492844014 Oxalosis type II en Synonym Active Only initial character case insensitive SNOMED CT core module
492845010 Primary hyperoxaluria type II en Synonym Active Only initial character case insensitive SNOMED CT core module
777685010 Primary hyperoxaluria, type II (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Primary hyperoxaluria, type II Is a Primary hyperoxaluria true Inferred relationship Existential restriction modifier
Primary hyperoxaluria, type II Finding site Kidney structure true Inferred relationship Existential restriction modifier 2
Primary hyperoxaluria, type II Occurrence Congenital true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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