249893002: Gross movement of body and limbs (observable entity)

SNOMED CT Concept\Observable entity (observable entity)\Movement observable\Gross movement of body and limbs

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Gross movement of body and limbs	Is a	Movement observable	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Isolated hereditary congenital facial paralysis (IHCFP) is an extremely rare neurological disorder presumed to result from maldevelopment of the facial nucleus and/or cranial nerve and has been reported in fewer than 10 families to date. It manifests as non-progressive, isolated, unilateral or bilateral, symmetrical or asymmetrical facial palsy. Involvement of the branches of the facial nerve can be unequal.	Interprets	False	Gross movement of body and limbs	Inferred relationship	Some	2
Flaccid monoplegia of upper limb (disorder)	Interprets	False	Gross movement of body and limbs	Inferred relationship	Some	1
Flaccid monoplegia of lower limb (disorder)	Interprets	False	Gross movement of body and limbs	Inferred relationship	Some	1
Right common peroneal nerve palsy	Interprets	True	Gross movement of body and limbs	Inferred relationship	Some	2
Left common peroneal nerve palsy	Interprets	True	Gross movement of body and limbs	Inferred relationship	Some	2
Paralysis of right radial nerve (finding)	Interprets	True	Gross movement of body and limbs	Inferred relationship	Some	2
Paralysis of left radial nerve (finding)	Interprets	True	Gross movement of body and limbs	Inferred relationship	Some	2
Paralysis of right vocal cord	Interprets	True	Gross movement of body and limbs	Inferred relationship	Some	1
Paralysis of left vocal cord (disorder)	Interprets	True	Gross movement of body and limbs	Inferred relationship	Some	1
A very rare congenital cranial dysinnervation disorder characterised by unilateral or bilateral non progressive congenital facial palsy (VII cranial nerve) with impairments of ocular abduction (VI cranial nerve). It can also be associated with other cranial nerves palsies, orofacial anomalies and limb defects.	Interprets	False	Gross movement of body and limbs	Inferred relationship	Some	1
A rare, slowly progressive genetic peripheral neuropathy characterized by distal atrophy and weakness affecting the upper limbs (with a predilection for the thenar eminence) and subsequently the lower limbs, associated with uni- or bilateral vocal cord paresis leading to hoarse voice and breathing difficulties, and facial weakness.	Interprets	True	Gross movement of body and limbs	Inferred relationship	Some	1
Vagus nerve laryngeal paralysis	Interprets	False	Gross movement of body and limbs	Inferred relationship	Some	1
Ptosis-vocal cord paralysis syndrome is a rare, hereditary disorder with ptosis characterized by the combination of congenital bilateral recurrent laryngeal nerve paralysis and congenital bilateral ptosis. There have been no further descriptions in the literature since 1983.	Interprets	False	Gross movement of body and limbs	Inferred relationship	Some	1
A rare genetic neuromuscular channelopathy characterized by normokalemic episodes of painful muscle cramping followed by progressive, permanent, flaccid weakness, triggered by stress, cold and exercise, associated with myopathic myopathy and painful acute edema with neuronal compression, foot drop and muscle degeneration when located in the tibialis anterior muscle group.	Interprets	True	Gross movement of body and limbs	Inferred relationship	Some	1
Periodic paralysis with later-onset distal motor neuropathy is a rare, genetic, neuromuscular disease characterized by acute episodic muscle weakness in upper and lower extremities (which responds to acetazolamide treatment) associated with later-onset, chronic, slowly progressive, distal, axonal neuropathy.	Interprets	True	Gross movement of body and limbs	Inferred relationship	Some	1
A rare peripheral neuropathy characterized by an acute onset of unilateral facial muscle weakness with Bell's phenomenon. It is non-progressive, resolves spontaneously, and it might be recurrent with no obvious precipitating factors.	Interprets	False	Gross movement of body and limbs	Inferred relationship	Some	1
Nerve palsy	Interprets	False	Gross movement of body and limbs	Inferred relationship	Some	1
Complete paralysis of left vocal cord	Interprets	True	Gross movement of body and limbs	Inferred relationship	Some	1
Complete paralysis of right vocal cord	Interprets	True	Gross movement of body and limbs	Inferred relationship	Some	1
Muscle paralysis due to and following neuromuscular blockade (disorder)	Interprets	True	Gross movement of body and limbs	Inferred relationship	Some	1
Palsy of vagus nerve (disorder)	Interprets	True	Gross movement of body and limbs	Inferred relationship	Some	1
Palsy of accessory nerve (disorder)	Interprets	True	Gross movement of body and limbs	Inferred relationship	Some	1
Palsy of glossopharyngeal nerve	Interprets	True	Gross movement of body and limbs	Inferred relationship	Some	1
Palsy of upper motor nerve	Interprets	True	Gross movement of body and limbs	Inferred relationship	Some	1
à l'examen : paralysie du motoneurone supérieur d'un nerf crânien	Interprets	False	Gross movement of body and limbs	Inferred relationship	Some	1
Palsy of laryngeal nerve due to birth trauma (disorder)	Interprets	True	Gross movement of body and limbs	Inferred relationship	Some	1
Paralysis of cervical sympathetic trunk (disorder)	Interprets	False	Gross movement of body and limbs	Inferred relationship	Some	2
Acute mastoiditis with facial paralysis	Interprets	False	Gross movement of body and limbs	Inferred relationship	Some	2
Cranial nerve palsy due to diabetes mellitus	Interprets	False	Gross movement of body and limbs	Inferred relationship	Some	2
Cranial nerve palsy due to type 1 diabetes mellitus	Interprets	False	Gross movement of body and limbs	Inferred relationship	Some	2
Cranial nerve palsy due to type 2 diabetes mellitus	Interprets	False	Gross movement of body and limbs	Inferred relationship	Some	2
Ophthalmoplegia due to diabetes mellitus (disorder)	Interprets	True	Gross movement of body and limbs	Inferred relationship	Some	2
A rare, localized variant of Guillain-Barré syndrome characterized by rapidly progressive bilateral facial nerve palsy, distal paresthesias, and minimal or no motor weakness. Deep tendon reflexes are usually diminished or absent but can be present or even exaggerated in rare cases. CSF analysis may reveal albuminocytologic dissociation. Nerve conduction velocity studies often show demyelinating type of neuropathy, although axonal polyneuropathy has been also described.	Interprets	False	Gross movement of body and limbs	Inferred relationship	Some	3
A rare X-linked syndromic intellectual disability characterized by congenital and permanent vocal cord paralysis causing severe congenital laryngeal stridor, associated with intellectual disability in male patients. Other presenting symptoms may include weak cry, cough, cyanosis, neonatal asphyxia, feeding difficulty, aspiration, and bronchiectasis. Microcephaly, tone abnormalities, visual and hearing impairment may also be associated features.	Interprets	True	Gross movement of body and limbs	Inferred relationship	Some	2
Bell's palsy	Interprets	False	Gross movement of body and limbs	Inferred relationship	Some	3
Common peroneal nerve paralysis (disorder)	Interprets	True	Gross movement of body and limbs	Inferred relationship	Some	2

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Id	Description	Lang	Type	Status	Case?	Module
372761012	Gross movement of body and limbs	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
640373019	Gross movement of body and limbs (observable entity)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1224312019	Observation of gross motor movement	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1224313012	General mobility	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
311131000077115	mobilité globale du tronc et des membres	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module