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

722968003: Acquired ataxia (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3334052018 Acquired ataxia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3334417017 Acquired ataxia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1841651000195110 atassia acquisita it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
968781000172110 ataxie acquise fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


5 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acquired ataxia Is a Ataxia true Inferred relationship Some
Acquired ataxia Is a Movement disorder true Inferred relationship Some
Acquired ataxia Finding site Structure of nervous system (body structure) false Inferred relationship Some 2
Acquired ataxia Occurrence Any period of life commencing after birth, but before death. true Inferred relationship Some 1
Acquired ataxia Finding site Structure of nervous system (body structure) true Inferred relationship Some 1
Acquired ataxia Interprets mouvement false Inferred relationship Some 2
Acquired ataxia Is a Disorder of nervous system (disorder) true Inferred relationship Some
Acquired ataxia Interprets Movement observable true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT) is a rare, acquired, neurological disease characterized by encephalopathy associated with elevated antithyroid antibodies, in the absence of other causes. Clinical presentation varies from minor cognitive impairment to status epilepticus and coma, and frequently includes seizures, confusion, speech disorder, memory impairment, ataxia and psychiatric manifestations. Is a False Acquired ataxia Inferred relationship Some
Ataxia due to chronic infection of central nervous system (disorder) Is a True Acquired ataxia Inferred relationship Some
A rare neuronal ceroid lipofuscinosis disorder characterized by juvenile-onset of progressive spinocerebellar ataxia, bulbar syndrome (manifesting with dysarthria, dysphagia and dysphonia), pyramidal and extrapyramidal involvement (including myoclonus, amyotrophy, unsteady gait, akinesia, rigidity, dysarthric speech) and intellectual deterioration. Muscle biopsy displays autofluorescent bodies and lipofuscin deposits in brain and, occasionally the retina, upon postmortem. Is a True Acquired ataxia Inferred relationship Some
Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome is a rare hereditary spastic ataxia disorder characterized by childhood onset of slowly progressive lower limb spastic paraparesis and cerebellar ataxia (with dysarthria, swallowing difficulties, motor degeneration), associated with sensorimotor neuropathy (including muscle weakness and distal amyotrophy in lower extremities) and progressive myoclonic epilepsy. Ocular signs (ptosis, oculomotor apraxia), dysmetria, dysdiadochokinesia, dystonic movements and myoclonus may also be associated. Is a False Acquired ataxia Inferred relationship Some
Ataxia due to disorder of immune function (disorder) Is a True Acquired ataxia Inferred relationship Some
Ataxia due to subpial siderosis (disorder) Is a True Acquired ataxia Inferred relationship Some
Ataxia due to acquired vitamin deficiency Is a False Acquired ataxia Inferred relationship Some
Acquired ataxia due to vitamin deficiency Is a True Acquired ataxia Inferred relationship Some

This concept is not in any reference sets

Back to Start