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725418006: syndrome de gigantisme cérébral-kystes maxillaires (trouble)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    3442476016 Cerebral gigantism jaw cysts syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3442477013 Cerebral gigantism jaw cysts syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3442478015 Cramer Niederdellmann syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    797771000241111 syndrome de gigantisme cérébral-kystes maxillaires (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
    876771000172113 syndrome de gigantisme cérébral-kystes maxillaires fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
    949781000172114 syndrome de Cramer-Niederdellmann fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
    3442479011 Syndrome that is characterized by cerebral gigantism associated with a jaw cyst basal cell nevoid syndrome. It has been reported in less than ten patients from two families. Neurological manifestations include hydrocephalus, ventricular malformation, a cerebellar syndrome, intracranial calcification, oculomotor disturbances and in some cases mild peripheral nervous disorders. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    3442480014 Syndrome that is characterised by cerebral gigantism associated with a jaw cyst basal cell naevoid syndrome. It has been reported in less than ten patients from two families. Neurological manifestations include hydrocephalus, ventricular malformation, a cerebellar syndrome, intracranial calcification, oculomotor disturbances and in some cases mild peripheral nervous disorders. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Cerebral gigantism jaw cysts syndrome (disorder) Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
    Cerebral gigantism jaw cysts syndrome (disorder) morphologie associée (attribut) structure anormale sur le plan morphologique false Inferred relationship Some 1
    Cerebral gigantism jaw cysts syndrome (disorder) est un(e) (attribut) Multiple malformation syndrome with early overgrowth (disorder) false Inferred relationship Some
    Cerebral gigantism jaw cysts syndrome (disorder) est un(e) (attribut) Congenital anomaly of central nervous system false Inferred relationship Some
    Cerebral gigantism jaw cysts syndrome (disorder) morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 1
    Cerebral gigantism jaw cysts syndrome (disorder) survenue (attribut) congénital false Inferred relationship Some 1
    Cerebral gigantism jaw cysts syndrome (disorder) localisation d'une constatation (attribut) Structure of central nervous system (body structure) false Inferred relationship Some 1

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

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