FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.4  |  FHIR Version n/a  User: [n/a]

702364003: Chylomicron retention disease (disorder)


Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2995184011 Chylomicron retention disease en Synonym Active Case insensitive SNOMED CT core
2995232014 Lipid transport defect of intestine en Synonym Active Case insensitive SNOMED CT core
2995490019 Chylomicron retention disease (disorder) en Fully specified name Active Case insensitive SNOMED CT core
2995599016 Anderson syndrome en Synonym Active Case insensitive SNOMED CT core
2995972013 An autosomal recessive disorder of severe fat malabsorption associated with failure to thrive in infancy. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chylomicron retention disease Is a Autosomal recessive hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start