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17901006: Primary hyperoxaluria (disorder)


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
30247019 Primary hyperoxaluria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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 Only initial character 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
3413171001000113 Hyperoxalurie, primäre de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
631441000172113 hyperoxalurie primaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
631441000172113 hyperoxalurie primaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3413171001000113 Hyperoxalurie, primäre de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


3 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Primary hyperoxaluria, type II Is a True Primary hyperoxaluria (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Primary hyperoxaluria, type I (disorder) Is a True Primary hyperoxaluria (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
[EDTA] Primary oxalosis associated with renal failure Is a False Primary hyperoxaluria (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Primary hyperoxaluria type III (disorder) Is a True Primary hyperoxaluria (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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