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40720005: Cerebral cyst (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Apr 2025. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    67919015 Cerebral cyst en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    492748017 Cerebral cysts en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    777418012 Cerebral cyst (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    348561000077119 kyste cérébral fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    kyste cérébral Is a Cyst of central nervous system false Inferred relationship Some
    kyste cérébral Is a lésion crânienne localisée false Inferred relationship Some
    kyste cérébral Finding site Brain structure false Inferred relationship Some 1
    kyste cérébral Associated morphology Cyst false Inferred relationship Some 1
    kyste cérébral Is a Intracranial mass false Inferred relationship Some
    kyste cérébral Is a Lesion of brain false Inferred relationship Some
    kyste cérébral Associated morphology Cyst false Inferred relationship Some 1
    kyste cérébral Finding site Brain structure false Inferred relationship Some 1
    kyste cérébral Is a Disorder of brain (disorder) false Inferred relationship Some
    kyste cérébral Is a Mass lesion of brain (finding) false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Ependymal cyst Is a False kyste cérébral Inferred relationship Some
    kyste cérébral congénital Is a False kyste cérébral Inferred relationship Some
    Porencephalic cyst Is a False kyste cérébral Inferred relationship Some
    Other specified cerebral cyst Is a False kyste cérébral Inferred relationship Some
    Cerebral cyst NOS Is a False kyste cérébral Inferred relationship Some
    Choroid plexus cyst Is a False kyste cérébral Inferred relationship Some
    Cyst of septum pellucidum Is a False kyste cérébral Inferred relationship Some
    Pituitary cyst Is a False kyste cérébral Inferred relationship Some
    Multicystic encephalomalacia Is a False kyste cérébral Inferred relationship Some
    Cyst of pineal gland (disorder) Is a False kyste cérébral Inferred relationship Some
    kyste hydatique cérébral Is a False kyste cérébral Inferred relationship Some
    Acquired periventricular cyst Is a False kyste cérébral Inferred relationship Some
    kyste dermoïde de l'encéphale Is a False kyste cérébral Inferred relationship Some
    Epidermoid cyst of brain Is a False kyste cérébral Inferred relationship Some
    Ependymal cyst of spinal cord (disorder) Is a False kyste cérébral Inferred relationship Some
    Benign neoplastic cyst of brain (disorder) Is a False kyste cérébral Inferred relationship Some
    Colloid brain cyst Is a False kyste cérébral Inferred relationship Some
    Ependymal cyst of ventricle of brain (disorder) Is a False kyste cérébral Inferred relationship Some
    A rare, nonprogressive, neurological disorder marked by intellectual deficit, spasticity and motor retardation associated with characteristic MRI findings of anterior bilateral temporal lobe cysts and multilobar leukoencephalopathy. So far, around 30 cases have been reported in the literature. Onset occurs in the first few months of life. Sensorineural deafness and microcephaly have also been reported. The etiology is unknown but an autosomal recessive mode of inheritance has been suggested. Is a False kyste cérébral Inferred relationship Some
    Cystic leukoencephalopathy without megalencephaly is characterized by non-progressive leukoencephalopathy, bilateral cysts in the anterior part of the temporal lobe, cerebral white matter anomalies and severe psychomotor impairment. Less than 50 patients have been described in the literature so far. Inheritance is most likely autosomal recessive. Is a False kyste cérébral Inferred relationship Some
    Dermoid cyst of brain (disorder) Is a False kyste cérébral Inferred relationship Some
    Cerebellar infectious cyst Is a False kyste cérébral Inferred relationship Some
    Infectious cyst of cerebral lobe Is a False kyste cérébral Inferred relationship Some
    A rare genetic cerebral small vessel disease characterized by leukoencephalopathy and cerebral calcification and cysts due to diffuse cerebral microangiopathy resulting in microcystic and macrocystic parenchymal degeneration. The condition can present at any age from early childhood to late adulthood and manifests as a progressive cerebral degeneration. Symptoms are variable, but restricted to the central nervous systems, and include, among others, slowing of cognitive performance, seizures, and movement disorder with a combination of pyramidal, extrapyramidal, and cerebellar features. Is a False kyste cérébral Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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