FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

1178005: Infantile spastic cerebral palsy (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    199351011 Infantile spastic cerebral palsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    693361019 Infantile spastic cerebral palsy (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
    Infantile spastic cerebral palsy Is a Spastic syndrome false Inferred relationship Some
    Infantile spastic cerebral palsy Is a A type of cerebral palsy defined by increased tone and pathological reflexes resulting in an abnormal pattern of movement and posture. false Inferred relationship Some
    Infantile spastic cerebral palsy Finding site The cerebrum is the regional structure of the brain, which is the adult equivalent of the forebrain or prosencephalon. It is constituted by the structural derivatives of the telencephalon and diencephalon including the cerebral hemispheres, epithalamus, thalamus, hypothalamus, lateral ventricles and third ventricle. This definition is harmonious with the Federation of Association of Anatomist Second Edition (2019) Part V Terminologia Anatomica. false Inferred relationship Some
    Infantile spastic cerebral palsy Is a Spastic syndrome (disorder) false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Cerebral palsy with spastic tetraparesis Is a False Infantile spastic cerebral palsy Inferred relationship Some
    A subtype of non-spastic cerebral palsy with involuntary, uncontrolled recurring, and occasionally stereotyped movements with a varying muscle tone; primitive reflex patterns predominate. Is a False Infantile spastic cerebral palsy Inferred relationship Some
    A subtype of non-spastic cerebral palsy with loss of muscular coordination with abnormal force and rhythm, and impairment of accuracy; commonly presents with gait and trunk ataxia, poor balance, past pointing, terminal intention tremor, scanning speech, nystagmus and other abnormal eye movements, and hypotonia. Low tone is a prominent feature. Is a False Infantile spastic cerebral palsy Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

    Back to Start