FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

29291001: Glycogen storage disease, type VI (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
49015012 Glycogen storage disease, type VI en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
49016013 Hepatic phosphorylase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
49017016 Hers disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
49018014 GSD VI en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
49019018 Hepatic glycogen phosphorylase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
760169015 Glycogen storage disease, type VI (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Glycogen storage disease, type VI est un(e) (attribut) Autosomal recessive hereditary disorder true Inferred relationship Some
Glycogen storage disease, type VI morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Glycogen storage disease, type VI localisation d'une constatation (attribut) système digestif false Inferred relationship Some 1
Glycogen storage disease, type VI est un(e) (attribut) Glycogen storage disease, hepatic form true Inferred relationship Some
Glycogen storage disease, type VI est un(e) (attribut) X-linked hereditary disease false Inferred relationship Some
Glycogen storage disease, type VI localisation d'une constatation (attribut) structure de muscle squelettique false Inferred relationship Some
Glycogen storage disease, type VI survenue (attribut) congénital true Inferred relationship Some 1
Glycogen storage disease, type VI morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 2
Glycogen storage disease, type VI localisation d'une constatation (attribut) foie true Inferred relationship Some 2
Glycogen storage disease, type VI localisation d'une constatation (attribut) organe digestif (structure corporelle) false Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start