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723125008: Epileptic encephalopathy (disorder)

Status: current, Primitive. 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 Case insensitive SNOMED CT core
3334667018 Epileptic encephalopathy en Synonym Active Case insensitive SNOMED CT core

17 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Epileptic encephalopathy Is a Generalised epilepsy true Inferred relationship Some
Epileptic encephalopathy Finding site Structure of cerebrum true Inferred relationship Some 1
Epileptic encephalopathy Has definitional manifestation Seizure false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome Is a True Epileptic encephalopathy Inferred relationship Some
Multiple congenital anomalies, hypotonia, seizures syndrome type 2 Is a True Epileptic encephalopathy Inferred relationship Some
Myoclonic epilepsy in non-progressive encephalopathy Is a True Epileptic encephalopathy Inferred relationship Some
KCNQ2-related neonatal epileptic encephalopathy Is a True Epileptic encephalopathy Inferred relationship Some
Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome Is a True Epileptic encephalopathy Inferred relationship Some
Lennox-Gastaut syndrome Is a True Epileptic encephalopathy Inferred relationship Some
Lethal neonatal spasticity, epileptic encephalopathy syndrome Is a True Epileptic encephalopathy Inferred relationship Some
SYNGAP1-related developmental and epileptic encephalopathy Is a True Epileptic encephalopathy Inferred relationship Some
RNF13-related severe early-onset epileptic encephalopathy Is a True Epileptic encephalopathy Inferred relationship Some
Neonatal epileptic encephalopathy due to glutaminase deficiency Is a True Epileptic encephalopathy Inferred relationship Some
CNTNAP2-related developmental and epileptic encephalopathy Is a True Epileptic encephalopathy Inferred relationship Some
CAD-CDG - carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation Is a True Epileptic encephalopathy Inferred relationship Some
Epileptic encephalopathy with global cerebral demyelination Is a True Epileptic encephalopathy Inferred relationship Some
Severe myoclonic epilepsy in infancy Is a True Epileptic encephalopathy Inferred relationship Some
Infantile epileptic dyskinetic encephalopathy Is a True Epileptic encephalopathy Inferred relationship Some

Reference Sets

Australian emergency department reference set

Queensland allied health clinical finding reference set

Queensland allied health indicator for intervention reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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