FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.24  |  FHIR Version n/a  User: [n/a]

1187522009: Peroxisome biogenesis disorder due to PEX26 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
4674073011 PEX26 deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
4674549014 Peroxisome biogenesis disorder due to PEX26 mutation en Synonym Active Only initial character case insensitive SNOMED CT core module
4674550014 Peroxisome biogenesis disorder due to PEX26 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 PEX26 mutation Is a Peroxisome biogenesis disorder true Inferred relationship Existential restriction modifier
Peroxisome biogenesis disorder due to PEX26 mutation Occurrence Congenital true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start