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783055005: Progressive myoclonic epilepsy type 5 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3757254019 Progressive myoclonic epilepsy type 5 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3757255018 PME type 5 - progressive myoclonic epilepsy type 5 en Synonym Active Entire term case sensitive SNOMED CT core module
3757256017 Progressive myoclonus epilepsy type 5 en Synonym Active Entire term case insensitive SNOMED CT core module
3757257014 Progressive myoclonic epilepsy type 5 en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Progressive myoclonic epilepsy type 5 Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Progressive myoclonic epilepsy type 5 Is a Chronic brain syndrome true Inferred relationship Existential restriction modifier
Progressive myoclonic epilepsy type 5 Is a Progressive myoclonic epilepsy true Inferred relationship Existential restriction modifier
Progressive myoclonic epilepsy type 5 Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Progressive myoclonic epilepsy type 5 Clinical course Progressive true Inferred relationship Existential restriction modifier 1
Progressive myoclonic epilepsy type 5 Finding site Structure of cerebrum true Inferred relationship Existential restriction modifier 2
Progressive myoclonic epilepsy type 5 Interprets Movement false Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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