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768666006: Syntaxin binding protein 1 encephalopathy with epilepsy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3686408013 STXBP1-related early-onset encephalopathy en Synonym Active Entire term case sensitive SNOMED CT core module
3686409017 Syntaxin binding protein 1 encephalopathy with epilepsy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3686410010 STXBP1 encephalopathy with epilepsy en Synonym Active Entire term case sensitive SNOMED CT core module
3686411014 STXBP1 (syntaxin binding protein 1) epileptic encephalopathy en Synonym Active Entire term case sensitive SNOMED CT core module
3686412019 Syntaxin binding protein 1 encephalopathy with epilepsy en Synonym Active Entire term case insensitive SNOMED CT core module
3686413012 Early infantile epileptic encephalopathy 4 en Synonym Active Entire term case insensitive SNOMED CT core module
3686414018 STXBP1-related epileptic encephalopathy en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Syntaxin binding protein 1 encephalopathy with epilepsy Occurrence Infancy true Inferred relationship Existential restriction modifier 1
Syntaxin binding protein 1 encephalopathy with epilepsy Finding site Structure of cerebrum true Inferred relationship Existential restriction modifier 1
Syntaxin binding protein 1 encephalopathy with epilepsy Is a Early infantile epileptic encephalopathy with suppression bursts 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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