1162508007: Motor function (finding)

SNOMED CT Concept\Clinical finding (finding)\Functional finding\Motor function

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

4589853014 Motor function en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

4589854015 Motor function (finding) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

6408181000241116 fonction motrice fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Motor function	Is a	Functional finding	true	Inferred relationship	Some
Motor function	Interprets	Motor function	true	Inferred relationship	Some	1
Motor function	Finding site	Structure of nervous system (body structure)	true	Inferred relationship	Some	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Equilibration disorder, vestibular nerve	Is a	True	Motor function	Inferred relationship	Some
Gastroparesis due to diabetes mellitus (disorder)	Is a	True	Motor function	Inferred relationship	Some
Neonatal hypokinesia	Is a	True	Motor function	Inferred relationship	Some
Rolandic epilepsy-speech dyspraxia syndrome is a rare, genetic epilepsy characterized by speech disorder (including a range of symptoms from dysarthria, speech dyspraxia, receptive and expressive language delay/regression and acquired aphasia to subtle impairments of conversational speech) and epilepsy (mostly focal and secondary generalized childhood-onset seizures, sometimes with aura). Mild to severe intellectual disability may also be observed.	Is a	True	Motor function	Inferred relationship	Some
Acquired choreiform dyspraxia	Is a	True	Motor function	Inferred relationship	Some
A rare genetic neurological disorder characterized by hypotonia, delayed motor development, dyskinesia of the limbs, intellectual disability with impaired speech development, seizures, autistic features, stereotypic movements, and sleep disturbance. Onset of symptoms is in infancy. Bilateral abnormalities in the putamen on brain MRI have been reported in some patients.	Is a	True	Motor function	Inferred relationship	Some
Cerebellar ataxia with quadrupedal gait	Is a	False	Motor function	Inferred relationship	Some
Cerebellar gait	Is a	True	Motor function	Inferred relationship	Some
Central core disease (CCD) is an inherited neuromuscular disorder characterised by central cores on muscle biopsy and clinical features of a congenital myopathy.	Is a	True	Motor function	Inferred relationship	Some

This concept is not in any reference sets