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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
5485201000241114 encéphalopathie épileptique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

17 descendants. Search Descendants:

Expanded Value Set

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

This concept is not in any reference sets

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