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702326000: Progressive myoclonus epilepsy with ataxia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2995418010 PRICKLE1-related progressive myoclonic epilepsy with ataxia en Synonym Active Entire term case sensitive SNOMED CT core module
2995588018 Progressive myoclonic epilepsy 1B en Synonym Active Only initial character case insensitive SNOMED CT core module
2995899014 Progressive myoclonus epilepsy with ataxia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2995906010 Progressive myoclonus epilepsy with ataxia 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 myoclonus epilepsy with ataxia Is a Progressive myoclonic epilepsy true Inferred relationship Existential restriction modifier
Progressive myoclonus epilepsy with ataxia Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Progressive myoclonus epilepsy with ataxia Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Progressive myoclonus epilepsy with ataxia Finding site Structure of cerebrum true Inferred relationship Existential restriction modifier 1
Progressive myoclonus epilepsy with ataxia Has definitional manifestation Seizure false Inferred relationship Existential restriction modifier
Progressive myoclonus epilepsy with ataxia Interprets Movement false 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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