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238059005: Disorder of peroxisomal function (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
356841014 Disorder of peroxisomal function en Synonym Active Entire term case insensitive SNOMED CT core module
626890017 Disorder of peroxisomal function (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


42 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Disorder of peroxisomal function Is a Inborn error of metabolism true Inferred relationship Existential restriction modifier
Disorder of peroxisomal function Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Disorder of peroxisomal function Finding site Body system structure false Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
General loss of peroxisomal function Is a True Disorder of peroxisomal function Inferred relationship Existential restriction modifier
Loss of multiple peroxisomal functions Is a True Disorder of peroxisomal function Inferred relationship Existential restriction modifier
Loss of single peroxisomal function Is a True Disorder of peroxisomal function Inferred relationship Existential restriction modifier
Peroxisome biogenesis disorder Is a True Disorder of peroxisomal function Inferred relationship Existential restriction modifier
Disorder of liver due to disorder of peroxisomal function Due to True Disorder of peroxisomal function Inferred relationship Existential restriction modifier 2

This concept is not in any reference sets

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