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15926001: Brainstem structure (body structure)


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
26973016 Brain stem en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
477581019 Brainstem structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
742848015 Brainstem structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5646671000241116 tronc cérébral fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5646681000241119 tronc de l'encéphale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5686381000241115 strucure du tronc de l'encéphale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


474 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Brainstem structure Is a Brain tissue structure false Inferred relationship Some
Brainstem structure Is a Infratentorial brain part (body structure) true Inferred relationship Some
Brainstem structure partie de Entire infratentorial brain false Additional relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Lesion of brainstem Finding site True Brainstem structure Inferred relationship Some 1
Neonatal brainstem dysfunction is a rare neurologic disease characterized by the association of suction-swallowing dysfunction, abnormal laryngeal sensitivity and motility manifesting with dyspnea or obstructive apnea-hypopnea. gastroesophageal reflux (generally resistant to medication) and cardiac vagal overactivity (e.g. brachycardia, vasovagal episodes) of varying degrees of severity. Impaired social interaction has also been reported. Finding site True Brainstem structure Inferred relationship Some 1
A rare, genetic, neurological disorder characterized by horizontal gaze palsy, sensorineural deafness, central hypoventilation, developmental delay, and intellectual disability, described in persons of Athabascan American Indian heritage. Swallowing dysfunction, vocal cord paralysis, facial paresis, seizures, internal carotid artery, and cardiac outflow tract anomalies may be additionally observed. No dysmorphic facial features are associated. Finding site True Brainstem structure Inferred relationship Some 1
CLIPPERS is a rare neuroinflammatory disorder characterized by brainstem-predominant encephalomyelitis which typically presents with cerebellar and cranial nerve manifestations (gait ataxia, dysarthria, visual disorders, parasthesias), as well as brainstem, myelopathy and cognitive findings, that respond to steroid treatment. Punctate curvilinear post-gadolinium contrast enhancement predominantly in the pons and cerebellum is observed on brain MRI and prominent, perivascular, CD3+ T-cell predominantly lymphocytic inflammation in neuropathology. Finding site True Brainstem structure Inferred relationship Some 2
Multiple sclerosis of the brainstem Finding site True Brainstem structure Inferred relationship Some 2
Injury of brain stem due to birth trauma (disorder) Finding site True Brainstem structure Inferred relationship Some 1
Abscess of brainstem (disorder) Finding site True Brainstem structure Inferred relationship Some 1
Focal traumatic hematoma of brainstem (disorder) Finding site True Brainstem structure Inferred relationship Some 1
Focal traumatic hemorrhage of brainstem (disorder) Finding site True Brainstem structure Inferred relationship Some 1
Granuloma of brainstem (disorder) Finding site True Brainstem structure Inferred relationship Some 1
Posterior inferior cerebellar artery syndrome Finding site True Brainstem structure Inferred relationship Some 3
Cerebellar pressure cone Finding site True Brainstem structure Inferred relationship Some 1
Brain stem laceration with concussion (disorder) Finding site True Brainstem structure Inferred relationship Some 1
Brain stem laceration with loss of consciousness (disorder) Finding site True Brainstem structure Inferred relationship Some 1
Traumatic hemorrhage of brainstem (disorder) Finding site True Brainstem structure Inferred relationship Some 1
Primary traumatic hemorrhage of brainstem (disorder) Finding site True Brainstem structure Inferred relationship Some 1
Secondary traumatic hemorrhage of brainstem (disorder) Finding site True Brainstem structure Inferred relationship Some 1
Focal non-hemorrhagic contusion of brainstem (disorder) Finding site True Brainstem structure Inferred relationship Some 3
Cerebrovascular accident of brainstem Finding site True Brainstem structure Inferred relationship Some 1
Focal laceration of brainstem (disorder) Finding site True Brainstem structure Inferred relationship Some 3
Primary glioblastoma multiforme of brainstem Finding site True Brainstem structure Inferred relationship Some 1
Primary astrocytoma of brain stem Finding site True Brainstem structure Inferred relationship Some 1
Primary malignant glioma of brainstem (disorder) Finding site True Brainstem structure Inferred relationship Some 1
Clinically isolated syndrome of brainstem (disorder) Finding site True Brainstem structure Inferred relationship Some 1
A rare genetic syndrome with a central nervous system malformation as a major feature, characterized by cortical malformations including posterior predominant lissencephaly and diffuse pachygyria, as well as midline crossing defects, thin corpus callosum, dysplastic hippocampi, narrowing of the brainstem with small pons and midbrain, widening of the medulla, and small cerebellum. Clinically, patients present global developmental delay, severe intellectual disability with poor or absent speech, axial hypotonia, and early-onset seizures, among others. Finding site True Brainstem structure Inferred relationship Some 2
Magnetic resonance imaging of brain and brain stem without contrast (procedure) Procedure site - Direct (attribute) True Brainstem structure Inferred relationship Some 1
Haemangioblastoma of brainstem Finding site True Brainstem structure Inferred relationship Some 1
Hyperintense lesion of brainstem on focal T2 magnetic resonance imaging (finding) Finding site True Brainstem structure Inferred relationship Some 1
Hypointense lesion of brainstem on focal T2 magnetic resonance imaging Finding site True Brainstem structure Inferred relationship Some 1
Congenital hypoplasia of brainstem Finding site True Brainstem structure Inferred relationship Some 1
Atrophy of brainstem Finding site True Brainstem structure Inferred relationship Some 1
A rare autoimmune encephalitis characterized by various phenotypes depending on the region of the brainstem that is involved; patients present with gaze palsies (in midbrain involvement), facial palsy or vertical gaze palsies (in pontine involvement), dysarthria, dysphagia or central hypoventilation (in medullary involvement). Additional clinical features may also involve pyramidal symptoms and gait impairment. Finding site True Brainstem structure Inferred relationship Some 1
Basilar migraine (disorder) Finding site True Brainstem structure Inferred relationship Some 1

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Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

Anatomy structure and part association reference set (foundation metadata concept)

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