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192990004: Benign myoclonic epilepsy in infancy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
297280011 Benign myoclonic epilepsy in infancy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
297281010 Neonatal myoclonic epilepsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
576829014 Benign myoclonic epilepsy in infancy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Benign myoclonic epilepsy in infancy est un(e) (attribut) épilepsie généralisée idiopathique true Inferred relationship Some
Benign myoclonic epilepsy in infancy est défini par la manifestation de (attribut) convulsion false Inferred relationship Some
Benign myoclonic epilepsy in infancy localisation d'une constatation (attribut) structure du cerveau true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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