FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.12  |  FHIR Version n/a  User: [n/a]

718750004: Component of oligomeric golgi complex 1 congenital disorder of glycosylation (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3313728015 CDG2G - carbohydrate deficient glycoprotein syndrome type 2G en Synonym Active Entire term case sensitive SNOMED CT core module
3313736012 Carbohydrate deficient glycoprotein syndrome type 2g en Synonym Active Entire term case insensitive SNOMED CT core module
3313737015 Carbohydrate deficient glycoprotein syndrome type IIg en Synonym Active Only initial character case insensitive SNOMED CT core module
3323076014 Component of oligomeric golgi complex 1 congenital disorder of glycosylation (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3323077017 COG1 congenital disorder of glycosylation en Synonym Active Entire term case sensitive SNOMED CT core module
3324357013 COG1 (component of oligomeric golgi complex 1) congenital disorder of glycosylation en Synonym Active Entire term case sensitive SNOMED CT core module
3324358015 Congenital disorder of glycosylation type IIg en Synonym Active Only initial character case insensitive SNOMED CT core module
3327884010 Component of oligomeric golgi complex 1 congenital disorder of glycosylation en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Component of oligomeric golgi complex 1 congenital disorder of glycosylation Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Component of oligomeric golgi complex 1 congenital disorder of glycosylation Is a Carbohydrate-deficient glycoprotein syndrome type II true Inferred relationship Existential restriction modifier
Component of oligomeric golgi complex 1 congenital disorder of glycosylation 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