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1187550009: Peroxisome biogenesis disorder due to PEX6 mutation (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4674131017 PEX6 deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
4674520018 Peroxisome biogenesis disorder due to PEX6 mutation en Synonym Active Only initial character case insensitive SNOMED CT core module
4674521019 Peroxisome biogenesis disorder due to PEX6 mutation (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Peroxisome biogenesis disorder due to PEX6 mutation Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Peroxisome biogenesis disorder due to PEX6 mutation Is a Peroxisome biogenesis disorder true 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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