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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


16 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Epileptic encephalopathy (disorder) est un(e) (attribut) Generalized epilepsy true Inferred relationship Some
Epileptic encephalopathy (disorder) localisation d'une constatation (attribut) structure du cerveau true Inferred relationship Some 1
Epileptic encephalopathy (disorder) est défini par la manifestation de (attribut) convulsion false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome (disorder) est un(e) (attribut) True Epileptic encephalopathy (disorder) Inferred relationship Some
Multiple congenital anomalies, hypotonia, seizures syndrome type 2 est un(e) (attribut) True Epileptic encephalopathy (disorder) Inferred relationship Some
Myoclonic epilepsy in non-progressive encephalopathy est un(e) (attribut) True Epileptic encephalopathy (disorder) Inferred relationship Some
Potassium voltage-gated channel subfamily Q member 2 related epileptic encephalopathy (disorder) est un(e) (attribut) True Epileptic encephalopathy (disorder) Inferred relationship Some
Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome est un(e) (attribut) True Epileptic encephalopathy (disorder) Inferred relationship Some
Lennox-Gastaut syndrome est un(e) (attribut) True Epileptic encephalopathy (disorder) Inferred relationship Some
Lethal neonatal spasticity, epileptic encephalopathy syndrome (disorder) est un(e) (attribut) True Epileptic encephalopathy (disorder) Inferred relationship Some
Synaptic Ras GTPase activating protein 1-related developmental and epileptic encephalopathy (disorder) est un(e) (attribut) True Epileptic encephalopathy (disorder) Inferred relationship Some
Ring finger protein 13-related severe early-onset epileptic encephalopathy (disorder) est un(e) (attribut) True Epileptic encephalopathy (disorder) Inferred relationship Some
Neonatal epileptic encephalopathy due to glutaminase deficiency est un(e) (attribut) True Epileptic encephalopathy (disorder) Inferred relationship Some
CNTNAP2-related developmental and epileptic encephalopathy est un(e) (attribut) True Epileptic encephalopathy (disorder) Inferred relationship Some
encéphalopathie épileptique avec démyélinisation cérébrale généralisée est un(e) (attribut) True Epileptic encephalopathy (disorder) Inferred relationship Some
Severe myoclonic epilepsy in infancy est un(e) (attribut) True Epileptic encephalopathy (disorder) Inferred relationship Some
Infantile epileptic dyskinetic encephalopathy (disorder) est un(e) (attribut) True Epileptic encephalopathy (disorder) Inferred relationship Some

This concept is not in any reference sets

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