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765089003: Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome (disorder)


Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3656366018 Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3656367010 Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome en Synonym Active Case insensitive SNOMED CT core
3656368017 Focal epilepsy, intellectual disability, dysarthria, ataxia syndrome en Synonym Active Case insensitive SNOMED CT core
3656177019 A rare genetic neurological disorder with early infantile-onset of seizures, borderline to moderate intellectual disability, cerebellar features including dysarthria and ataxia and cerebellar atrophy and cortical thickening observed on MRI imaging. Seizures are typically focal (with prominent eye blinking, facial and limb jerking), precipitated by fever and often commence with an oral sensory aura. When not properly controlled by anti-epileptic medication, weekly frequency and persistence into adult life is observed. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome Interprets Intellectual ability true Inferred relationship Some 2
Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome Has interpretation Impaired true Inferred relationship Some 2
Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome Interprets Adaptation behaviour true Inferred relationship Some 3
Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome Has interpretation Impaired true Inferred relationship Some 3
Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome Is a Partial seizure true Inferred relationship Some
Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome Is a Multiple system malformation syndrome true Inferred relationship Some
Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome Is a Intellectual disability true Inferred relationship Some
Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome Is a Dysgenesis of the cerebellum true Inferred relationship Some
Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome Is a Hereditary disorder of nervous system true Inferred relationship Some
Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome Associated morphology Developmental abnormality false Inferred relationship Some 1
Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome Occurrence Congenital true Inferred relationship Some 1
Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome Finding site Cerebellar structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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