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67305007: Familial essential myoclonus (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
111825012 Familial essential myoclonus en Synonym Active Entire term case insensitive SNOMED CT core module
807015010 Familial essential myoclonus (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1232917010 Essential myoclonus 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
Familial essential myoclonus Is a Myoclonic disorder true Inferred relationship Existential restriction modifier
Familial essential myoclonus Is a Extrapyramidal disease true Inferred relationship Existential restriction modifier
Familial essential myoclonus Finding site Extrapyramidal system structure true Inferred relationship Existential restriction modifier 1
Familial essential myoclonus Finding site Structure of muscle tissue false Inferred relationship Existential restriction modifier
Familial essential myoclonus Finding site Skeletal and/or smooth muscle structure false Inferred relationship Existential restriction modifier
Familial essential myoclonus Interprets Movement true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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