25087005: Structure of nervous system (body structure)

SNOMED CT Concept\Body structure (body structure)\Anatomical or acquired body structure (body structure)\Anatomical structure\Body system structure\Structure of nervous system (body structure)

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
Structure of nervous system (body structure)	Is a	Structure of nervous system organ AND/OR special sense organ	false	Inferred relationship	Some
Structure of nervous system (body structure)	partie de	Entire body as a whole	false	Additional relationship	Some
Structure of nervous system (body structure)	Is a	Body system structure	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Reversal of neuromuscular blockade	Procedure site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Neurological pain disorder	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Neuromuscular diagnostic procedure	Procedure site	False	Structure of nervous system (body structure)	Inferred relationship	Some	3
Axillary freckling due to neurofibromatosis (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
Muscle paralysis (procedure)	Procedure site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Tetanus neonatorum (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
Physical medicine neuromuscular training (procedure)	Procedure site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
Dysmorphic sialidosis, infantile form	Finding site	False	Structure of nervous system (body structure)	Inferred relationship	Some	1
Induced termination of pregnancy complicated by tetanus	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Tetanus omphalitis	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
The occurrence of abnormal involuntary movements that are incongruent with a known neurologic cause and are significantly improved on neurological exam with distraction or non-physiologic maneuvers. The disorder is defined by its clinical appearance, rather than by any causative speculation.	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Tracheal dyskinesia (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Tetanus	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
schwannomatose	Finding site	False	Structure of nervous system (body structure)	Inferred relationship	Some	2
Neurofibromatosis type 1	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Neuromuscular procedure	Procedure site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Paralysis of uvula after diphtheria (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Sleep-related movement disorder caused by drug	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
Sleep-related movement disorder caused by substance	Finding site	False	Structure of nervous system (body structure)	Inferred relationship	Some	2
Transient motor tic (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
Neurotoxicity caused by snake venom (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Cerebral sarcoidosis	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
Localised tetanus	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
A rare genetic, neuro-ophthalmological disease characterized by progressive weakness of the external eye muscles, resulting in bilateral ptosis and diffuse symmetric ophthalmoparesis. Additional signs may include skeletal muscle weakness, cataracts, hearing loss, sensory axonal neuropathy, ataxia, parkinsonism, cardiomyopathy, hypogonadism and depression. It is usually less severe than autosomal recessive form.	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
A rare genetic, neuro-ophthalmological disease characterized by progressive weakness of the external eye muscles, resulting in bilateral ptosis and diffuse, symmetric ophthalmoparesis. Additional signs may include generalized skeletal muscle weakness, muscle atrophy, sensory axonal neuropathy, ataxia, cardiomyopathy, and psychiatric symptoms. It is usually more severe than autosomal dominant form.	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
Normal vibration sensation of left foot (finding)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	3
Normal vibration sensation of right foot (finding)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	3
Absence of vibratory sense	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
Absence of vibration sense of right foot	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	3
Absence of vibration sense of left foot	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	3
Decreased vibratory sense (finding)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
Connectomic imaging (procedure)	Procedure site - Direct (attribute)	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
MEGDEL syndrome is a rare, genetic, neurometabolic disorder characterised by neonatal hypoglycaemia, features of sepsis that are not linked to infection, development of feeding problems, failure to thrive, transient liver dysfunction, and truncal hypotonia followed by dystonia and spasticity which results in psychomotor development arrest and/or regression. Progressive sensorineural deafness, intellectual disability and absent speech are also associated. Laboratory tests demonstrate 3-methylglutaconic aciduria and temporary elevated serum lactate and transaminases.	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Generalised tetanus	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Autoimmune opsoclonus myoclonus	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
Maroteaux-Lamy syndrome	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Maroteaux-Lamy syndrome, severe form	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Maroteaux-Lamy syndrome, intermediate form	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Maroteaux-Lamy syndrome, mild form (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Intact motor nervous system	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Neuronal ceroid lipofuscinosis 8	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Chronic infectious disease of central nervous system	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Toxic chorea (disorder)	Finding site	False	Structure of nervous system (body structure)	Inferred relationship	Some	1
Ataxia due to chronic infection of central nervous system (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
Acquired ataxia	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Nervous system implant	This attribute represents the site where the device is intended to reside in or on the body.	True	Structure of nervous system (body structure)	Inferred relationship	Some
Ventricular reservoir	This attribute represents the site where the device is intended to reside in or on the body.	True	Structure of nervous system (body structure)	Inferred relationship	Some
Ommaya reservoir	This attribute represents the site where the device is intended to reside in or on the body.	True	Structure of nervous system (body structure)	Inferred relationship	Some
Rickham reservoir	This attribute represents the site where the device is intended to reside in or on the body.	True	Structure of nervous system (body structure)	Inferred relationship	Some
Subcutaneous cerebrospinal fluid reservoir	This attribute represents the site where the device is intended to reside in or on the body.	True	Structure of nervous system (body structure)	Inferred relationship	Some
Cranial port/reservoir (physical object)	This attribute represents the site where the device is intended to reside in or on the body.	True	Structure of nervous system (body structure)	Inferred relationship	Some
Total ophthalmoplegia of left eye (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
Total ophthalmoplegia of right eye (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
Bilateral total ophthalmoplegia	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	4
Motor neuron disease due to lead intoxication (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
Bilateral progressive external ophthalmoplegia	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	3
Neurovascular injury (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Absence of sensation due to conversion disorder	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
17q11 microdeletion syndrome is a rare severe form of neurofibromatosis type 1 characterized by mild facial dysmorphism, developmental delay, intellectual disability, increased risk of malignancies, and a large number of neurofibromas.	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	3
A rare complex overgrowth syndrome characterised by progressive overgrowth of the skeleton, skin, adipose, and central nervous systems.	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
Port-wine stain in proteus syndrome (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	3
Segmental neurofibromatosis type 1 (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Intracranial hemorrhage following injury with prolonged loss of consciousness AND return to pre-existing conscious level	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	6
Intracranial hemorrhage following injury with prolonged loss of consciousness without return to pre-existing conscious level	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	6
Paralysis of left side of tongue	Finding site	False	Structure of nervous system (body structure)	Inferred relationship	Some	2
Paralysis of right side of tongue (disorder)	Finding site	False	Structure of nervous system (body structure)	Inferred relationship	Some	2
Secondary syphilis of nervous system	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Hereditary ataxia (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
A rare, genetic, autosomal dominant spastic ataxia disorder characterized by lower-limb spasticity and ataxia in the form of head jerks, ocular movement abnormalities, dysarthria, dysphagia and gait disturbances.	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
A rare genetic disease characterized by mild intellectual deficit, congenital cataract, progressive sensorineural hearing impairment, ataxia, peripheral neuropathy, and short stature. There have been no further descriptions in the literature since 1991.	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	5
Marie's cerebellar ataxia	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Episodic ataxia type 2 (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Episodic ataxia type 1 (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Episodic ataxia (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
A rare, X-linked syndromic intellectual disability disorder characterized by non-progressive ataxia, apraxia, variable intellectual disability and/or visuospatial, visuographic and visuoconstructive dysfunctions in male patients. Seizures, congenital clubfoot and macroorchidism have also been associated. Partial clinical expression was noted in obligate female carriers. There have been no further descriptions in the literature since 1992.	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	3
Episodic ataxia with slurred speech is a rare hereditary ataxia characterized by recurrent episodes of ataxia with variable frequency and duration, associated with slurred speech, generalized muscle weakness and balance disturbance. Other symptoms may occur between episodes, including intention tremor, gait ataxia, mild dysarthria, myokymia, migraine and nystagmus.	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
Ataxia co-occurrent and due to abetalipoproteinemia (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
A rare complex overgrowth syndrome characterised by progressive overgrowth of the skeleton, skin, adipose, and central nervous systems.	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	4
Fibrous skin tumor of tuberous sclerosis	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	4
Sturge-Weber syndrome	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	3
Cerebral-retinal arteriovenous aneurysm (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
Pulmonary tuberous sclerosis (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	5
Ash leaf spot, tuberous sclerosis (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	3
Hereditary neurocutaneous angiomata (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	4
Port-wine stain in proteus syndrome (disorder)	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	5
Phakomatosis cesioflammea	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
Phakomatosis spilorosea	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
Phakomatosis caesiomarmorata	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
A rare contiguous gene syndrome involving a partial deletion of chromosome 16 and characterized by early-onset and severe polycystic kidney disease with various manifestations of tuberous sclerosis (multiple angiomyolipomas, lymphangioleiomyomatosis and periventricular calcifications of the central nervous system).	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	5
PENS syndrome is a rare, genetic, neurocutaneous syndrome characterized by the presence of randomly distributed, small, white to yellowish, multiple, rounded or irregular polycyclically-shaped, epidermal keratotic papules and plaques of gem-like appearance with a rough surface, typically located on the trunk and proximal limbs, associated with variable neurological abnormalities, including psychomotor delay, epilepsy, speech and language impairment and attention deficit-hyperactivity disorder. Clumsiness, dyslexia and ophthalmological abnormalities have also been reported.	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	3
A rare, genetic, neurocutaneous disease characterized by severe developmental abnormalities of the nervous system and aberrant differentiation of the epidermis. Patients present with a unique constellation of clinical signs described with the acronym CEDNIK: CErebral Dysgenesis, Neuropathy, Ichthyosis, and palmoplantar Keratoderma.	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	6
A rare neurocutaneous syndrome characterized by the association of cerebellum (rhombencephalosynapsis), cranial nerves (trigeminal anesthesia), and scalp (alopecia) abnormalities. Other features observed in patients were craniosynostosis, midfacial hypoplasia, bilateral corneal opacities, low-set ears, short stature, moderate intellectual impairment and ataxia. Hyperactivity, depression, self-injurious behavior and bipolar disorder have also been reported.	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	3
A rare genetic neurological disease characterized by silvery hair, profound dysfunction of central nervous system, abnormal melanocytes and melanosomes and abnormal inclusion bodies in fibroblast and other cells.	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	3
Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome is a rare, genetic pigmentation anomaly of the skin disorder characterized by congenital hypomelanotic and hypermelanotic cutaneous macules associated with, in some patients, retarded growth and intellectual disability. There have been no further descriptions in the literature since 1978.	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	3
Drug-induced dyskinesia, acute onset	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	2
Drug-induced dyskinesia	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Tardive dyskinesia	Finding site	True	Structure of nervous system (body structure)	Inferred relationship	Some	1
Neuromuscular diagnostic procedure	Procedure site - Direct (attribute)	False	Structure of nervous system (body structure)	Inferred relationship	Some	2
Sensory perception is a function that endows a person with the capacity to detect internal and external stimuli via sensory transducer structures in the body and transmit this information to the brain (sensory function), then cognitively represent, organize, and interpret this information (perception function). The realization of the sensory perception function is the acquisition of information from stimuli both within the body and the external environment.	This attribute specifies the location of the entity specified by the attribute "Inheres in".	False	Structure of nervous system (body structure)	Inferred relationship	Some	1
Neurovascular assessment of upper limb	Procedure site - Direct (attribute)	True	Structure of nervous system (body structure)	Inferred relationship	Some	2

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Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

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Id	Description	Lang	Type	Status	Case?	Module
42045011	Nervous system	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
482830017	Nervous system structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2638392011	Structure of nervous system (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2642423017	Structure of nervous system	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
12601000077114	structure du système nerveux	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
1001561000241118	système nerveux	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module