21483005: Structure of central 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 subdivision of organ system (body structure)\Structure of subdivision of nervous system (body structure)\Structure of central nervous system (body structure)

\Structure of nervous system (body structure)\Structure of subdivision of nervous system (body structure)\Structure of central 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 central nervous system (body structure)	Is a	Entire subdivision of nervous system (body structure)	false	Inferred relationship	Some
Structure of central nervous system (body structure)	partie de	Entire nervous system	false	Additional relationship	Some
Structure of central nervous system (body structure)	Is a	Structure of nervous system (body structure)	false	Inferred relationship	Some
Structure of central nervous system (body structure)	Is a	Structure of subdivision of nervous system (body structure)	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Intracranial hypotension due to cerebrospinal fluid rhinorrhoea	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Needling of hydrocephalic head (procedure)	Procedure site - Direct (attribute)	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Transabdominal encephalocentesis of fetal head	Procedure site - Direct (attribute)	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Encephalocentesis	Procedure site - Direct (attribute)	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Paracentesis of central nervous system structure	Procedure site - Direct (attribute)	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Primary gliosarcoma of central nervous system	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Primary anaplastic astrocytoma of central nervous system (disorder)	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Primary malignant atypical teratoid rhabdoid neoplasm of central nervous system	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Primary astroblastoma of central nervous system (disorder)	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Primary anaplastic oligodendroglioma of central nervous system (disorder)	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Primary anaplastic ependymoma of central nervous system	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Primary giant cell glioblastoma of central nervous system	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Primary gemistocytic astrocytoma of central nervous system (disorder)	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Primary medulloepithelioma of central nervous system (disorder)	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Primary fibrillary astrocytoma of central nervous system	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Lyme neuroborreliosis (disorder)	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
A rare developmental defect during embryogenesis characterized by unilateral duplication of an eye which may appear as a synophthalmic eye in a single orbit or as two separate unilateral eyes, each in a separate orbit. The malformation is always associated with other anomalies of the central nervous system (such as porencephaly, meningocele, or arachnoidal cysts) and with craniofacial abnormalities. A proboscis is often found. Clinically, moderate mental retardation and epilepsy are typical.	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	2
Chronic central neuropathic pain due to spinal cord injury (disorder)	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	2
Chronic central neuropathic pain due to brain injury	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	2
Chronic central neuropathic pain due to multiple sclerosis (disorder)	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	2
Oligodendroglioma of central nervous system (disorder)	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Disorder of central nervous system due to and following procedure (disorder)	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	2
Central nervous tissue	Is a	True	Structure of central nervous system (body structure)	Inferred relationship	Some
Neurocutaneous melanosis	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	2
PPM-X syndrome	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Primary malignant melanoma of central nervous system (disorder)	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Amplitude integrated electroencephalography (procedure)	Procedure site - Direct (attribute)	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
A rare genetic neurological syndrome of variable severity with characteristics of progressive spasticity affecting predominantly the lower limbs. Most patients manifest global developmental delay, moderate to severe intellectual disability and white matter abnormalities in infancy complicated by variable features including seizures, episodic respiratory failure, joint contractures and ocular problems. Some patients have normal early development until later childhood followed by regression in motor, cognitive and language skills over time. Some patients manifest only spastic paraplegia.	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
A rare multiple congenital anomalies/dysmorphic syndrome characterized by central nervous system abnormalities (particularly cerebellar hypoplasia), congenital microcephaly, intellectual disability, severe neurodevelopmental delay, growth impairment, dystonia, eye abnormalities (particularly cataract whereas retinal dystrophy and Leber congenital amaurosis are also reported) and congenital dyserythropoietic anemia. Additional clinical features may include other structural brain abnormalities (such as cerebral atrophy, basal ganglia atrophy, brainstem hypoplasia), feeding difficulties, sleep disturbances, hepatomegaly, and sensorineural deafness.	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	2
Presence of regression of primary malignant neoplasm of central nervous system after neoadjuvant antineoplastic therapy (observable entity)	This attribute specifies the location of the entity specified by the attribute "Inheres in".	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Neuromuscular scoliosis due to and following poliomyelitis (disorder)	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	3
Neuromuscular scoliosis of cervical and thoracic spine due to and following poliomyelitis (disorder)	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	4
A rare genetic neurodegenerative disease with characteristics of childhood-onset severe developmental delay with regression, poor motor development, speech impairment and hypotonia due to CLCN6 mutations. Most of the patients have vision abnormalities, respiratory system abnormalities (including chronic respiratory insufficiency and tracheostomy that may lead to ventilator dependency) and feeding difficulties (percutaneous endoscopic gastronomy). Skin abnormalities including hyperhidrosis can be present.	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Thoracolumbar neuromuscular scoliosis due to and following poliomyelitis	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	4
Central nervous system disorder due to Sjögren's syndrome	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Hemangioblastoma of central nervous system (disorder)	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
A rare interstitial lung disease characterized by early-onset, severe, progressive lung disease manifesting by respiratory distress, neurological symptoms including axial hypotonia, developmental delay, irritability, dystonia, poor visual contact and seizures, and variable multisystemic involvement including malabsorption, progressive growth failure, recurrent infections, chronic hemolytic anemia and liver dysfunction. Kidney dysfunction, cardiac involvement including cardiomegaly and cardiac hypertrophy, decreased vision and strabismus have also been reported. Lung fibrosis may cause death in infancy from respiratory failure.	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Central nervous system neurostimulator (physical object)	This attribute represents the site where the device is intended to reside in or on the body.	True	Structure of central nervous system (body structure)	Inferred relationship	Some
Brown-Séquard syndrome due to multiple sclerosis	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Brown-Séquard syndrome due to multiple sclerosis	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	2
A rare central nervous system embryonal tumour characterised by embryonal cells arranged in multilayered rosettes and displaying one of three morphological patterns: embryonal tumour with abundant neuropil and true rosettes, ependymoblastoma, or medulloepithelioma. The tumours typically have a C19MC alteration or (rarely) a DICER1 mutation and correspond to WHO grade IV. They are mostly localised intracranially, rarely in the spinal cord, and commonly cause signs and symptoms of elevated intracranial pressure, sometimes seizures and focal neurological signs. Most cases occur in children during the first two years of life.	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Central nervous system dysfunction in newborn	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Head lag in newborn (disorder)	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1
Central core disease (CCD) is an inherited neuromuscular disorder characterised by central cores on muscle biopsy and clinical features of a congenital myopathy.	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	2
Autosomal recessive central core disease	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	2
Autosomal dominant central core disease (disorder)	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	2
Mitochondrial complex I deficiency nuclear type 10 (disorder)	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	3
Early-onset neurodegeneration, choreoathetoid movement, microcytic anemia due to iron responsive element binding protein 2 gene mutation (disorder)	Finding site	True	Structure of central nervous system (body structure)	Inferred relationship	Some	1

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Reference Sets

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

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

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Id	Description	Lang	Type	Status	Case?	Module
36053015	Central nervous system	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
481035013	Central nervous system structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2638268018	Structure of central nervous system (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2642337010	Structure of central nervous system	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
278861000077111	structure du système nerveux central	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
959871000172115	systema nervosum centrale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
1002691000172114	système nerveux central	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module