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6204001: juveniele 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
11300012 Juvenile myoclonic epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
801169016 Juvenile myoclonic epilepsy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1232274015 JME - Juvenile myoclonic epilepsy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
524491000146118 juveniele myoklonische epilepsie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
683191000146111 juveniele myoclonusepilepsie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
11491621000146117 juveniele myoklonische epilepsie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
5232443018 A type of epilepsy that presents with myoclonic epileptic seizures, usually between 10 and 24 years of age, in an otherwise normal adolescent or adult. Generalized tonic-clonic seizures occur in greater than 90 percent of individuals and absence seizures occur in a third. Seizures typically occur shortly after waking and when tired. Sleep deprivation is an important provoking factor. Photosensitivity is common. Development and cognition are typically normal. Neurological examination is normal. The electroencephalogram shows 3 to 5.5 Hz generalized spike-wave and polyspike-wave and a normal background. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5232444012 A type of epilepsy that presents with myoclonic epileptic seizures, usually between 10 and 24 years of age, in an otherwise normal adolescent or adult. Generalised tonic-clonic seizures occur in greater than 90 percent of individuals and absence seizures occur in a third. Seizures typically occur shortly after waking and when tired. Sleep deprivation is an important provoking factor. Photosensitivity is common. Development and cognition are typically normal. Neurological examination is normal. The electroencephalogram shows 3 to 5.5 Hz generalised spike-wave and polyspike-wave and a normal background. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Juvenile myoclonic epilepsy Is a myoklonische aanval false Inferred relationship Some
Juvenile myoclonic epilepsy Is a Idiopathic generalized epilepsy true Inferred relationship Some
Juvenile myoclonic epilepsy Finding site Muscle tissue false Inferred relationship Some
Juvenile myoclonic epilepsy Finding site Cerebrum false Inferred relationship Some 1
Juvenile myoclonic epilepsy Has definitional manifestation Seizure false Inferred relationship Some
Juvenile myoclonic epilepsy Finding site Skeletal and/or smooth muscle structure (body structure) false Inferred relationship Some
Juvenile myoclonic epilepsy Interprets Movement false Inferred relationship Some 2
Juvenile myoclonic epilepsy Finding site Brain structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
therapieresistente juveniele myoklonische epilepsie Is a False Juvenile myoclonic epilepsy Inferred relationship Some

This concept is not in any reference sets

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