FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

445252005: Glucose transporter protein type 1 deficiency syndrome (disorder)


Status: current, Primitive. Date: 31-Jul 2010. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2869027015 Glucose transporter protein type 1 deficiency syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
2872335013 Glucose transporter protein type 1 deficiency syndrome en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Glucose transporter protein type 1 deficiency syndrome Is a Metabolic encephalopathy true Inferred relationship Some
Glucose transporter protein type 1 deficiency syndrome Is a Hereditary disorder of nervous system true Inferred relationship Some
Glucose transporter protein type 1 deficiency syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Glucose transporter protein type 1 deficiency syndrome Finding site Brain structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Epilepsy due to glucose transporter protein type 1 deficiency syndrome Due to True Glucose transporter protein type 1 deficiency syndrome Inferred relationship Some 2

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start