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267581004: progressieve myoklonische epilepsie (aandoening)


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

Descriptions:

Id Description Lang Type Status Case? Module
399395015 Progressive myoclonic epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
660215010 Progressive myoclonic epilepsy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
77621000146111 progressieve myoklonische epilepsie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
966011000146110 progressieve myoklonische epilepsie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


14 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Progressive myoclonic epilepsy Is a cryptogene gegeneraliseerde epilepsie (aandoening) false Inferred relationship Some
Progressive myoclonic epilepsy Finding site Cerebrum false Inferred relationship Some 1
Progressive myoclonic epilepsy Has definitional manifestation Seizure false Inferred relationship Some
Progressive myoclonic epilepsy Is a myoklonische aanval false Inferred relationship Some
Progressive myoclonic epilepsy Is a tonisch-klonische epilepsie (aandoening) false Inferred relationship Some
Progressive myoclonic epilepsy Is a Generalized epilepsy false Inferred relationship Some
Progressive myoclonic epilepsy Interprets Movement false Inferred relationship Some 2
Progressive myoclonic epilepsy Finding site Brain structure true Inferred relationship Some 1
Progressive myoclonic epilepsy Is a Epilepsy true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Unverricht-Lundborg syndrome Is a True Progressive myoclonic epilepsy Inferred relationship Some
Lafora disease Is a True Progressive myoclonic epilepsy Inferred relationship Some
Progressive myoclonus epilepsy with ataxia (disorder) Is a True Progressive myoclonic epilepsy Inferred relationship Some
Spinal muscular atrophy with progressive myoclonic epilepsy (disorder) Is a True Progressive myoclonic epilepsy Inferred relationship Some
Early-onset Lafora body disease (disorder) Is a True Progressive myoclonic epilepsy Inferred relationship Some
Progressive myoclonic epilepsy with dystonia Is a True Progressive myoclonic epilepsy Inferred relationship Some
Action myoclonus renal failure syndrome Is a True Progressive myoclonic epilepsy Inferred relationship Some
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) Is a True Progressive myoclonic epilepsy Inferred relationship Some
Progressive myoclonic epilepsy type 8 (disorder) Is a True Progressive myoclonic epilepsy Inferred relationship Some
Progressive myoclonic epilepsy type 3 Is a True Progressive myoclonic epilepsy Inferred relationship Some
Progressive myoclonic epilepsy type 6 (disorder) Is a True Progressive myoclonic epilepsy Inferred relationship Some
Progressive myoclonic epilepsy type 5 (disorder) Is a True Progressive myoclonic epilepsy Inferred relationship Some
Progressive myoclonic epilepsy type 7 Is a True Progressive myoclonic epilepsy Inferred relationship Some
Progressive myoclonic epilepsy type 9 Is a True Progressive myoclonic epilepsy Inferred relationship Some

This concept is not in any reference sets

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