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1365681000: Paraneoplastic isolated brainstem encephalitis (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
5454280019 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5454281015 A rare autoimmune encephalitis characterised 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5454276012 Paraneoplastic isolated brainstem encephalitis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5454277015 Paraneoplastic isolated brainstem encephalitis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5454284011 Paraneoplastic isolated rhombencephalitis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5454285012 Paraneoplastic isolated rhomboencephalitis en Synonym (core metadata concept) 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
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. Is a Brainstem encephalitis true Inferred relationship Some
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. Is a Paraneoplastic encephalitis (disorder) true Inferred relationship Some
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. Is a Autoimmune encephalitis true Inferred relationship Some
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. Due to Neoplastic disease true Inferred relationship Some 3
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 Brainstem structure true 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. Associated morphology Inflammatory morphology (morphologic abnormality) true 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. Pathological process (attribute) Autoimmune process true 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 Brain tissue structure true Inferred relationship Some 2
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. Associated morphology Inflammatory morphology (morphologic abnormality) true Inferred relationship Some 2
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. Pathological process (attribute) Autoimmune process true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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