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763770005: Familial myoclonus of cerebral cortex (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3643773010 Familial cortical myoclonus en Synonym Active Entire term case insensitive SNOMED CT core module
3643777011 Familial myoclonus of cerebral cortex en Synonym Active Entire term case insensitive SNOMED CT core module
3643778018 Familial myoclonus of cerebral cortex (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial myoclonus of cerebral cortex Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Familial myoclonus of cerebral cortex Is a Familial disease true Inferred relationship Existential restriction modifier
Familial myoclonus of cerebral cortex Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Familial myoclonus of cerebral cortex Is a Cerebral cortex myoclonus true Inferred relationship Existential restriction modifier
Familial myoclonus of cerebral cortex Finding site Structure of cerebral cortex true Inferred relationship Existential restriction modifier 1
Familial myoclonus of cerebral cortex 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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