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40951006: Primary hyperoxaluria, type II (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
492842013 Deficiency of glyoxylate reductase en Synonym Active Case insensitive SNOMED CT core
492843015 Deficiency of glycerate dehydrogenase en Synonym Active Case insensitive SNOMED CT core
492844014 Oxalosis type II en Synonym Active Initial character case insensitive SNOMED CT core
492845010 Primary hyperoxaluria type II en Synonym Active Initial character case insensitive SNOMED CT core
68304013 Primary hyperoxaluria, type II en Synonym Active Initial character case insensitive SNOMED CT core
68305014 Glyoxylate reductase deficiency en Synonym Active Case insensitive SNOMED CT core
68306010 Glyceric dehydrogenase deficiency en Synonym Active Case insensitive SNOMED CT core
68307018 L-glyceric aciduria en Synonym Active Case sensitive SNOMED CT core
68308011 Glycerate dehydrogenase deficiency en Synonym Active Case insensitive SNOMED CT core
777685010 Primary hyperoxaluria, type II (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core


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 Some
Primary hyperoxaluria, type II Finding site Kidney structure true Inferred relationship Some 2
Primary hyperoxaluria, type II Occurrence Congenital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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