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84757009: Epilepsy (disorder)


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
178739011 Epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
826667014 Epilepsy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5180629012 A disease of the brain characterized by an enduring predisposition to generate epileptic seizures. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5180630019 A disease of the brain characterised by an enduring predisposition to generate epileptic seizures. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
398161000172110 épilepsie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
82861000172116 epilepsie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
1891731000172112 morbus caducus nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


242 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Epilepsy Is a Seizure disorder true Inferred relationship Some
Epilepsy Finding site Cerebrum false Inferred relationship Some 1
Epilepsy Has definitional manifestation Seizure false Inferred relationship Some
Epilepsy Finding site Brain structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Familial infantile myoclonic epilepsy Is a True Epilepsy Inferred relationship Some
Epilepsy due to congenital infectious disease (disorder) Is a True Epilepsy Inferred relationship Some
Epilepsy due to glucose transporter protein type 1 deficiency syndrome (disorder) Is a True Epilepsy Inferred relationship Some
Epilepsy due to Rasmussen syndrome (disorder) Is a True Epilepsy Inferred relationship Some
Epilepsy due to perinatal intraventricular haemorrhage Is a True Epilepsy Inferred relationship Some
Epilepsy due to perinatal cerebral ischemia (disorder) Is a True Epilepsy Inferred relationship Some
Epilepsy due to perinatal periventricular hemorrhage (disorder) Is a True Epilepsy Inferred relationship Some
Malignant migrating partial seizures of infancy (disorder) Is a True Epilepsy Inferred relationship Some
Benign infantile seizure with mild gastroenteritis syndrome (disorder) Is a True Epilepsy Inferred relationship Some
Developmental and epileptic encephalopathy Is a True Epilepsy Inferred relationship Some
Epileptic encephalopathy (disorder) Is a True Epilepsy Inferred relationship Some
Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome Is a True Epilepsy Inferred relationship Some
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency (disorder) Is a True Epilepsy Inferred relationship Some
West syndrome Is a True Epilepsy Inferred relationship Some
Progressive myoclonic epilepsy Is a True Epilepsy Inferred relationship Some

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Reference Sets

Belgian GP subset (foundation metadata concept)

Belgian subset for medical problems in patient health records

GB English

US English

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