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17901006: primaire hyperoxalurie (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
30247019 Primary hyperoxaluria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
30250016 Primary oxalosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
745258015 Primary hyperoxaluria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
341151000146118 primaire hyperoxalurie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
341161000146115 primaire hyperoxalurie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
10301551000146110 Erfelijke stofwisselingsziekte die ontstaat door een overschot aan oxaalzuur of oxalaten in de urine; deze ziekte kan nierstenen en nierverkalking veroorzaken. nl Definition Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Primary hyperoxaluria Is a Hereditary disorder of the urinary system false Inferred relationship Some
Primary hyperoxaluria Is a Inborn error of metabolism true Inferred relationship Some
Primary hyperoxaluria Is a Metabolic renal disease true Inferred relationship Some
Primary hyperoxaluria Is a Disorder of carbohydrate metabolism true Inferred relationship Some
Primary hyperoxaluria Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Primary hyperoxaluria Is a Enzymopathy true Inferred relationship Some
Primary hyperoxaluria Is a Congenital anomaly of trunk false Inferred relationship Some
Primary hyperoxaluria Finding site Kidney structure true Inferred relationship Some 2
Primary hyperoxaluria Occurrence Congenital true Inferred relationship Some 1
Primary hyperoxaluria Is a Hereditary nephropathy (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Primary hyperoxaluria, type II Is a True Primary hyperoxaluria Inferred relationship Some
Primary hyperoxaluria, type I Is a True Primary hyperoxaluria Inferred relationship Some
[EDTA] Primary oxalosis associated with renal failure Is a False Primary hyperoxaluria Inferred relationship Some
Primary hyperoxaluria type III (disorder) Is a True Primary hyperoxaluria Inferred relationship Some
primaire hyperoxalurie type 3 (aandoening) Is a False Primary hyperoxaluria Inferred relationship Some

This concept is not in any reference sets

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