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828971000000101: Primary hyperoxaluria, type III (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 01-Apr 2012. Module: SNOMED CT United Kingdom clinical extension module

Descriptions:

Id Description Lang Type Status Case? Module
2154911000000110 Primary hyperoxaluria, type III en Synonym Active Only initial character case insensitive SNOMED CT United Kingdom clinical extension module
2154921000000116 Primary hyperoxaluria, type III (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT United Kingdom clinical extension module
2257941000000115 Oxalosis type 3 en Synonym Active Only initial character case insensitive SNOMED CT United Kingdom clinical extension module
2257951000000117 4-hydroxy-2-oxoglutarate aldolase deficiency en Synonym Active Only initial character case insensitive SNOMED CT United Kingdom clinical extension module


0 descendants.

Expanded Value Set


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