722968003: Acquired ataxia (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Finding of movement\Movement disorder\Acquired ataxia

\Finding related to coordination / incoordination (finding)\Ataxia\Acquired ataxia

\Disease\Disorder of body system\Disorder of nervous system (disorder)\Acquired ataxia
\Disease\Movement disorder\Acquired ataxia

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

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	Movement	true	Inferred relationship	Some	2
Acquired ataxia	Is a	Disorder of nervous system (disorder)	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
A rare acquired neurological disease with characteristics of 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 with characteristics of juvenile-onset 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 post mortem.	Is a	True	Acquired ataxia	Inferred relationship	Some
A rare hereditary spastic ataxia disorder with 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. Caused by homozygous mutation in the AFG3L2 gene on chromosome 18p11.	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