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733115009: Congenital disorder of glycosylation type 1y (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3498784013 Signal sequence receptor subunit 4 congenital disorder of glycosylation en Synonym Active Entire term case insensitive SNOMED CT core module
3498785014 Congenital disorder of glycosylation type Iy en Synonym Active Only initial character case insensitive SNOMED CT core module
3498786010 SSR4-CDG - signal sequence receptor subunit 4 congenital disorder of glycosylation en Synonym Active Entire term case sensitive SNOMED CT core module
3498787018 Congenital disorder of glycosylation type 1y en Synonym Active Only initial character case insensitive SNOMED CT core module
3498788011 Carbohydrate deficient glycoprotein syndrome type Iy en Synonym Active Only initial character case insensitive SNOMED CT core module
3498789015 Congenital disorder of glycosylation type 1y (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
Congenital disorder of glycosylation type 1y Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
Congenital disorder of glycosylation type 1y Is a Carbohydrate-deficient glycoprotein syndrome type I true Inferred relationship Existential restriction modifier
Congenital disorder of glycosylation type 1y Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital disorder of glycosylation type 1y Is a X-linked recessive hereditary disease 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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