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432171000124102: Severe myoclonic epilepsy in infancy, refractory (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Mar 2025. Module: US National Library of Medicine maintained module (core metadata concept)

    Descriptions:

    Id Description Lang Type Status Case? Module
    627421000124110 Severe myoclonic epilepsy in infancy, refractory (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) US National Library of Medicine maintained module (core metadata concept)
    627431000124113 Severe myoclonic epilepsy in infancy, refractory en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) US National Library of Medicine maintained module (core metadata concept)
    627441000124115 Severe myoclonic epilepsy in infancy, intractable en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) US National Library of Medicine maintained module (core metadata concept)
    627451000124118 Dravet syndrome, refractory en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) US National Library of Medicine maintained module (core metadata concept)
    627461000124116 Dravet syndrome, intractable en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) US National Library of Medicine maintained module (core metadata concept)


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Severe myoclonic epilepsy in infancy, refractory Is a Severe myoclonic epilepsy in infancy false Inferred relationship Some
    Severe myoclonic epilepsy in infancy, refractory Is a Refractory epilepsy false Inferred relationship Some
    Severe myoclonic epilepsy in infancy, refractory Finding site Cerebrum false Inferred relationship Some
    Severe myoclonic epilepsy in infancy, refractory Occurrence Infancy false Inferred relationship Some
    Severe myoclonic epilepsy in infancy, refractory Occurrence Childhood false Inferred relationship Some
    Severe myoclonic epilepsy in infancy, refractory Has definitional manifestation Seizure false Inferred relationship Some
    Severe myoclonic epilepsy in infancy, refractory Is a Refractory idiopathic generalized epilepsy false Inferred relationship Some
    Severe myoclonic epilepsy in infancy, refractory Occurrence Infancy false Inferred relationship Some 1
    Severe myoclonic epilepsy in infancy, refractory Finding site Cerebrum false Inferred relationship Some 1
    Severe myoclonic epilepsy in infancy, refractory Interprets Movement false Inferred relationship Some 2
    Severe myoclonic epilepsy in infancy, refractory Is a Drug resistance to anti-seizure medication (disorder) false Inferred relationship Some
    Severe myoclonic epilepsy in infancy, refractory Associated with Drug or medicament (substance) false Inferred relationship Some 2
    Severe myoclonic epilepsy in infancy, refractory Finding site Brain structure false Inferred relationship Some 1
    Severe myoclonic epilepsy in infancy, refractory Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    POSSIBLY REPLACED BY association reference set (foundation metadata concept)

    Concept inactivation indicator reference set

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