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

709412006: Congenital disorder of glycosylation type 1c (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3039537015 Carbohydrate deficient glycoprotein syndrome type V en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3039747015 Congenital disorder of glycosylation type 1c (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3039904012 Congenital disorder of glycosylation type 1c en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3040291014 Carbohydrate deficient glycoprotein syndrome type 1c en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital disorder of glycosylation type 1c (disorder) Is a Carbohydrate-deficient glycoprotein syndrome type I true Inferred relationship Some
Congenital disorder of glycosylation type 1c (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Congenital disorder of glycosylation type 1c (disorder) Occurrence Congenital true Inferred relationship Some 2
Congenital disorder of glycosylation type 1c (disorder) Due to Deficiency of glucosyltransferase 1 true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start