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723125008: Epileptic encephalopathy (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
3334666010 Epileptic encephalopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3334667018 Epileptic encephalopathy en Synonym Active Entire term case insensitive SNOMED CT core module

17 descendants. Search Descendants:

Expanded Value Set

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

This concept is not in any reference sets

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