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715534008: Infantile convulsion and choreoathetosis syndrome (disorder)


Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1673881000168117 ICCA (infantile convulsion and choreoathetosis) syndrome en Synonym Active Case sensitive SNOMED Clinical Terms Australian extension
3302956017 Infantile convulsion and choreoathetosis syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3302957014 Infantile convulsion and choreoathetosis syndrome en Synonym Active Case insensitive SNOMED CT core
3302958016 ICCA syndrome en Synonym Active Case sensitive SNOMED CT core
3302959012 Paroxysmal kinesigenic dyskinesia and infantile convulsion en Synonym Active Case insensitive SNOMED CT core
3302960019 A rare neurological condition with manifestation of seizures during the first year of life and choreoathetotic dyskinetic attacks during childhood or adolescence. Benign familial infantile epilepsy begins at 3 to 12 months of age with a family history of the same type of seizures. Seizures are afebrile and normally disappear after the first year of life. During childhood or adolescence, affected individuals present with paroxysmal kinesigenic dyskinesia with frequent and recurrent episodic choreathetotic or dystonic movements that last less than 1 minute. Can present as sporadic or familial, in the latter case, it is transmitted as an autosomal dominant trait that can be variably expressed within the same family. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Infantile convulsion and choreoathetosis syndrome Interprets Movement true Inferred relationship Some 4
Infantile convulsion and choreoathetosis syndrome Is a Benign neonatal convulsions true Inferred relationship Some
Infantile convulsion and choreoathetosis syndrome Is a Paroxysmal kinesigenic dyskinesia true Inferred relationship Some
Infantile convulsion and choreoathetosis syndrome Occurrence Neonatal true Inferred relationship Some 1
Infantile convulsion and choreoathetosis syndrome Clinical course Acute true Inferred relationship Some 3
Infantile convulsion and choreoathetosis syndrome Finding site Basal ganglion structure true Inferred relationship Some 2
Infantile convulsion and choreoathetosis syndrome Has definitional manifestation Seizure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

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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