FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

723125008: Epileptic encephalopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3334666010 Epileptic encephalopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3334667018 Epileptic encephalopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5243445018 EE - epileptic encephalopathy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5224371018 A type of epilepsy characterised by frequent epileptiform activity associated with developmental slowing and often regression on the background of previously normal development. In this type of epilepsy the frequent seizures and/or epileptiform discharges, rather than underlying aetiology is thought to be the only cause of developmental impairment. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5224372013 A type of epilepsy characterized by frequent epileptiform activity associated with developmental slowing and often regression on the background of previously normal development. In this type of epilepsy the frequent seizures and/or epileptiform discharges, rather than underlying etiology is thought to be the only cause of developmental impairment. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Epileptic encephalopathy (disorder) Is a Generalized epilepsy false Inferred relationship Some
Epileptic encephalopathy (disorder) Finding site Cerebrum false Inferred relationship Some 1
Epileptic encephalopathy (disorder) Has definitional manifestation Seizure false Inferred relationship Some
Epileptic encephalopathy (disorder) Is a Neurodevelopmental disorder true Inferred relationship Some
Epileptic encephalopathy (disorder) Is a Epilepsy true Inferred relationship Some
Epileptic encephalopathy (disorder) Finding site Brain structure true Inferred relationship Some 1
Epileptic encephalopathy (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Epileptic encephalopathy with global cerebral demyelination (disorder) Is a False Epileptic encephalopathy (disorder) Inferred relationship Some
Severe myoclonic epilepsy in infancy Is a False Epileptic encephalopathy (disorder) Inferred relationship Some
Infantile epileptic dyskinetic encephalopathy (disorder) Is a False Epileptic encephalopathy (disorder) Inferred relationship Some
Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome (disorder) Is a False Epileptic encephalopathy (disorder) Inferred relationship Some
Multiple congenital anomalies, hypotonia, seizures syndrome type 2 Is a False Epileptic encephalopathy (disorder) Inferred relationship Some
Myoclonic epilepsy in non-progressive encephalopathy Is a False Epileptic encephalopathy (disorder) Inferred relationship Some
Potassium voltage-gated channel subfamily Q member 2 related epileptic encephalopathy (disorder) Is a False Epileptic encephalopathy (disorder) Inferred relationship Some
Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome Is a False Epileptic encephalopathy (disorder) Inferred relationship Some
Lennox-Gastaut syndrome Is a False Epileptic encephalopathy (disorder) Inferred relationship Some
Lethal neonatal spasticity, epileptic encephalopathy syndrome (disorder) Is a False Epileptic encephalopathy (disorder) Inferred relationship Some
Synaptic Ras GTPase activating protein 1-related developmental and epileptic encephalopathy (disorder) Is a False Epileptic encephalopathy (disorder) Inferred relationship Some
Ring finger protein 13-related severe early-onset epileptic encephalopathy (disorder) Is a False Epileptic encephalopathy (disorder) Inferred relationship Some
Neonatal epileptic encephalopathy due to glutaminase deficiency Is a False Epileptic encephalopathy (disorder) Inferred relationship Some
CNTNAP2-related developmental and epileptic encephalopathy Is a False Epileptic encephalopathy (disorder) Inferred relationship Some
Carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation (disorder) Is a False Epileptic encephalopathy (disorder) Inferred relationship Some
Rasmussen syndrome Is a True Epileptic encephalopathy (disorder) Inferred relationship Some
Febrile infection related epilepsy syndrome (disorder) Is a True Epileptic encephalopathy (disorder) Inferred relationship Some

This concept is not in any reference sets

Back to Start