113305005: Cerebellar structure (body structure)

SNOMED CT Concept\Body structure (body structure)\Anatomical or acquired body structure (body structure)\Anatomical structure\...

\Anatomical structure which has as its parts a heterogeneous collection of organs, organ parts, cells, cell parts or body part subdivisions that are adjacent to, or continuous with one another; does not constitute a cell part, cell, tissue, organ, or body part subdivision.\Structure of anatomical compartment (body structure)\Intracranial structure (body structure)\Brain structure\Brain part\...

\Brain region\Infratentorial brain structure\Infratentorial brain part (body structure)\Cerebellar structure

\Extrapyramidal system structure (body structure)\Cerebellar structure

\Body region structure\Body part structure\Upper body structure\Upper body part structure\Structure of head and/or neck (body structure)\Head structure\Head part\Intracranial structure (body structure)\Brain structure\Brain part\...

\Brain region\Infratentorial brain structure\Infratentorial brain part (body structure)\Cerebellar structure

\Extrapyramidal system structure (body structure)\Cerebellar 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
Cerebellar structure	Is a	Infratentorial brain structure	false	Inferred relationship	Some
Cerebellar structure	Is a	Extrapyramidal system structure (body structure)	true	Inferred relationship	Some
Cerebellar structure	Is a	Hindbrain structure	false	Inferred relationship	Some
Cerebellar structure	partie de	Entire infratentorial brain	false	Additional relationship	Some
Cerebellar structure	partie de	Entire extrapyramidal system	false	Additional relationship	Some
Cerebellar structure	Is a	Infratentorial brain part (body structure)	true	Inferred relationship	Some
Cerebellar structure	Is a	Brain tissue structure	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Cerebellar hemorrhage	Finding site	True	Cerebellar structure	Inferred relationship	Some	1
Cerebellar laceration with open intracranial wound AND no loss of consciousness	Finding site	False	Cerebellar structure	Inferred relationship	Some	1
Cerebellar laceration without open intracranial wound	Finding site	False	Cerebellar structure	Inferred relationship	Some	1
Cerebellar laceration with open intracranial wound AND prolonged loss of consciousness (more than 24 hours) AND return to pre-existing conscious level	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar laceration without open intracranial wound AND with no loss of consciousness	Finding site	False	Cerebellar structure	Inferred relationship	Some	1
Cerebellar laceration with open intracranial wound AND brief loss of consciousness (less than one hour)	Finding site	False	Cerebellar structure	Inferred relationship	Some	1
Cerebellar laceration with open intracranial wound AND loss of consciousness	Finding site	False	Cerebellar structure	Inferred relationship	Some	1
Cerebellar laceration with open intracranial wound AND moderate loss of consciousness (1-24 hours)	Finding site	False	Cerebellar structure	Inferred relationship	Some	2
Cerebellar laceration with open intracranial wound AND prolonged loss of consciousness (more than 24 hours) without return to pre-existing conscious level	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar laceration with open intracranial wound AND concussion	Finding site	False	Cerebellar structure	Inferred relationship	Some	1
Cerebellar hemangioblastomatosis	Finding site	False	Cerebellar structure	Inferred relationship	Some	1
Cerebellar laceration with open intracranial wound	Finding site	True	Cerebellar structure	Inferred relationship	Some	1
Roussy-Lévy syndrome	Finding site	False	Cerebellar structure	Inferred relationship	Some	1
Hereditary cerebellar degeneration	Finding site	False	Cerebellar structure	Inferred relationship	Some	1
Specimen from cerebellum (specimen)	Specimen source topography	True	Cerebellar structure	Inferred relationship	Some	1
Medulloblastoma of cerebellum	Finding site	False	Cerebellar structure	Inferred relationship	Some	1
Superior cerebellar artery syndrome (disorder)	Finding site	True	Cerebellar structure	Inferred relationship	Some	2
Sporadic olivopontocerebellar atrophy (disorder)	Finding site	False	Cerebellar structure	Inferred relationship	Some	1
Sporadic olivopontocerebellar atrophy (disorder)	Finding site	True	Cerebellar structure	Inferred relationship	Some	1
Malignant neoplasm of cerebellum (disorder)	Finding site	True	Cerebellar structure	Inferred relationship	Some	1
Cerebellar laceration with open intracranial wound AND no loss of consciousness	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar contusion without open intracranial wound AND with loss of consciousness	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar contusion with open intracranial wound AND loss of consciousness	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar (nontraumatic) and posterior fossa hemorrhage of fetus and newborn	Finding site	False	Cerebellar structure	Inferred relationship	Some	2
Cerebellar contusion with open intracranial wound AND prolonged loss of consciousness (more than 24 hours) without return to pre-existing conscious level	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar contusion with open intracranial wound AND no loss of consciousness	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar laceration without open intracranial wound	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar contusion without open intracranial wound AND with concussion	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar contusion without open intracranial wound AND with prolonged loss of consciousness (more than 24 hours) AND return to pre-existing conscious level	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar laceration without open intracranial wound AND with brief loss of consciousness (less than one hour)	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Biopsy of lesion of cerebellum (procedure)	Procedure site - Direct (attribute)	True	Cerebellar structure	Inferred relationship	Some	2
Cerebellar laceration without open intracranial wound AND with moderate loss of consciousness (1-24 hours)	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar contusion without open intracranial wound AND with brief loss of consciousness (less than one hour)	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar laceration with open intracranial wound AND prolonged loss of consciousness (more than 24 hours) AND return to pre-existing conscious level	Finding site	False	Cerebellar structure	Inferred relationship	Some	4
Cerebellar contusion with open intracranial wound AND prolonged loss of consciousness (more than 24 hours) AND return to pre-existing conscious level	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar contusion with open intracranial wound AND moderate loss of consciousness (1-24 hours)	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar contusion without open intracranial wound	Finding site	False	Cerebellar structure	Inferred relationship	Some	2
Cerebellar laceration with open intracranial wound AND concussion	Finding site	True	Cerebellar structure	Inferred relationship	Some	3
Cerebellar contusion without open intracranial wound AND with prolonged loss of consciousness (more than 24 hours) without return to pre-existing conscious level	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar laceration with open intracranial wound AND prolonged loss of consciousness (more than 24 hours) without return to pre-existing conscious level	Finding site	False	Cerebellar structure	Inferred relationship	Some	4
Cerebellar laceration without open intracranial wound AND with prolonged loss of consciousness (more than 24 hours) without return to pre-existing conscious level	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar contusion with open intracranial wound AND brief loss of consciousness (less than one hour)	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar laceration without open intracranial wound AND with concussion	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar contusion without open intracranial wound AND with moderate loss of consciousness (1-24 hours)	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar contusion with open intracranial wound	Finding site	False	Cerebellar structure	Inferred relationship	Some	1
Cerebellar contusion without open intracranial wound AND with no loss of consciousness	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar laceration with open intracranial wound AND moderate loss of consciousness (1-24 hours)	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar laceration with open intracranial wound AND loss of consciousness	Finding site	True	Cerebellar structure	Inferred relationship	Some	3
Cerebellar laceration without open intracranial wound AND with no loss of consciousness	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar contusion with open intracranial wound AND concussion	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar laceration without open intracranial wound AND with loss of consciousness	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar laceration without open intracranial wound AND with prolonged loss of consciousness (more than 24 hours) AND return to pre-existing conscious level	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Cerebellar laceration with open intracranial wound AND brief loss of consciousness (less than one hour)	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Spontaneous cerebellar haemorrhage	Finding site	True	Cerebellar structure	Inferred relationship	Some	1
Hereditary sensory-motor neuropathy, type V	Finding site	False	Cerebellar structure	Inferred relationship	Some	1
Myoclonic epilepsy myopathy sensory ataxia (disorder)	Finding site	False	Cerebellar structure	Inferred relationship	Some	4
Huntington disease-like syndrome	Finding site	False	Cerebellar structure	Inferred relationship	Some	1
Dentate dysplasia	Finding site	False	Cerebellar structure	Inferred relationship	Some	2
Cerebellar cortical dysplasia	Finding site	False	Cerebellar structure	Inferred relationship	Some	2
A rare genetic developmental and neurological disorder characterised by the association of partial bilateral aniridia (or iris hypoplasia), with non-progressive cerebellar ataxia, intellectual disability, and congenital hypotonia.	Finding site	True	Cerebellar structure	Inferred relationship	Some	2
Congenital cerebellar hypoplasia	Finding site	False	Cerebellar structure	Inferred relationship	Some	2
Dysgenesis of the cerebellum	Finding site	False	Cerebellar structure	Inferred relationship	Some	2
Congenital abnormal shape of cerebellum	Finding site	False	Cerebellar structure	Inferred relationship	Some	2
Congenital pontocerebellar hypoplasia	Finding site	False	Cerebellar structure	Inferred relationship	Some	2
Aplasia of cerebellum	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Anomalies of cerebellum	Finding site	False	Cerebellar structure	Inferred relationship	Some	2
Agenesis of cerebellum	Finding site	False	Cerebellar structure	Inferred relationship	Some	2
Infantile ascending hereditary spastic paralysis (disorder)	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Congenital cerebellar hypoplasia	Finding site	True	Cerebellar structure	Inferred relationship	Some	1
Spastic paraplegia type 15	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Spinocerebellar ataxia type 36 (disorder)	Finding site	True	Cerebellar structure	Inferred relationship	Some	2
Cerebellar contusion with open intracranial wound AND concussion	Finding site	True	Cerebellar structure	Inferred relationship	Some	2
Cerebellar neoplasm specimen (specimen)	Specimen source topography	True	Cerebellar structure	Inferred relationship	Some	1
Malignant glioma of cerebellum (disorder)	Finding site	True	Cerebellar structure	Inferred relationship	Some	1
A form of hereditary spastic ataxia characterised by an onset usually in adulthood (but ranging from 10-72 years) of progressive bilateral lower limb weakness and spasticity and sometimes predominant cerebellar ataxia. In addition to frequent sphincter dysfunction and decreased vibratory sense at the ankles, manifestations may include optical neuropathy, nystagmus, blepharoptosis, ophthalmoplegia, decreased hearing, scoliosis, pes cavus, motor and sensory neuropathy, muscle atrophy, parkinsonism, and dystonia.	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder)	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
A rare form of lissencephaly with cerebellar hypoplasia characterized by subtle microcephaly, hypotonia and neurological and cognitive development delay. Hippocampal malformation is a characteristic imaging feature of this disorder.	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death.	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
A rare form of lissencephaly with cerebellar hypoplasia characterized by pronounced microcephaly (<= -3 SD), intellectual disability, spastic diplegia and moderate to severe cerebellar hypoplasia involving both vermis and hemispheres.	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
A severe form of lissencephaly with cerebellar hypoplasia, characterized by a microcephaly of at least - 3 SD and a thick cortex associated with complete absence of the corpus callosum.	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
A complex hereditary spastic paraplegia characterized by progressive lower limbs weakness and spasticity, upper limbs weakness, dysarthria, hypomimia, sphincter disturbances, peripheral neuropathy, learning difficulties, cognitive impairment and dementia. Magnetic resonance imaging shows thin corpus callosum, cerebral atrophy, and periventricular white matter changes.	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
An autosomal dominant cerebellar ataxia type II that is characterized by progressive ataxia, motor system abnormalities, dysarthria, dysphagia and retinal degeneration leading to progressive blindness.	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Spinocerebellar ataxia type 1 (SCA1) is a subtype of type I autosomal dominant cerebellar ataxia characterized by dysarthria, writing difficulties, limb ataxia, and commonly nystagmus and saccadic abnormalities.	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Spinocerebellar ataxia type 2 (SCA2) is a subtype of type I autosomal dominant cerebellar ataxia characterized by truncal ataxia, dysarthria, slowed saccades and less commonly ophthalmoparesis and chorea.	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
An autosomal dominant cerebellar ataxia type III that is characterized by late-onset and slowly progressive gait ataxia and other cerebellar signs such as impaired muscle coordination and nystagmus.	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Spinocerebellar ataxia type 8 (SCA8) is a subtype of type I autosomal dominant cerebellar ataxia characterized by cerebellar ataxia and cognitive dysfunction in almost three quarters of patients and pyramidal and sensory signs in approximately a third of patients.	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Spinocerebellar ataxia type 10 (SCA10) is a subtype of type I autosomal dominant cerebellar ataxia. It is characterized by slowly progressive cerebellar syndrome and epilepsy, sometimes mild pyramidal signs, peripheral neuropathy and neuropsychological disturbances.	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Spinocerebellar ataxia type 4 (SCA4) is a very rare progressive and untreatable subtype of type I autosomal dominant cerebellar ataxia characterized by ataxia with sensory neuropathy.	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
Richards-Rundle syndrome is an extremely rare neurodegenerative disorder characterized by progressive spinocerebellar ataxia, sensorineural hearing loss, and hypergonadotropic hypogonadism associated with additional neurological manifestations (such as peripheral muscle wasting, nystagmus, intellectual disability or dementia) and ketoaciduria.	Finding site	False	Cerebellar structure	Inferred relationship	Some	4
A rare autosomal recessive cerebellar ataxia characterized by early onset of non- or slowly progressive cerebellar signs and symptoms including truncal and gait ataxia, dysarthria, dysmetria, dysdiadochokinesis, tremor, and nystagmus. Delayed psychomotor development and intellectual disability are variable. Additional reported features are spasticity, hypotonia, cataracts, and sensorineural hearing loss, among others. Brain imaging shows cerebellar atrophy.	Finding site	True	Cerebellar structure	Inferred relationship	Some	4
A rare autosomal recessive cerebellar ataxia characterized by early onset of non- or slowly progressive cerebellar signs and symptoms including truncal and gait ataxia, dysarthria, dysmetria, dysdiadochokinesis, tremor, and nystagmus. Delayed psychomotor development and intellectual disability are variable. Additional reported features are spasticity, hypotonia, cataracts, and sensorineural hearing loss, among others. Brain imaging shows cerebellar atrophy.	Finding site	False	Cerebellar structure	Inferred relationship	Some	5
A rare syndromic cerebellar ataxia characterized by hypodontia and sparse hair in combination with cerebellar ataxia and normal intelligence. Imaging demonstrates a cerebellar atrophy.	Finding site	False	Cerebellar structure	Inferred relationship	Some
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder)	Finding site	False	Cerebellar structure	Inferred relationship	Some	2
A rare, hereditary ataxia disorder characterized by the presence of spastic ataxia in association with bilateral congenital cataract, macular corneal dystrophy (stromal with deposition of mucoid material) and nonaxial myopia. Patients present normal intellectual development. There have been no further descriptions in the literature since 1986.	Finding site	True	Cerebellar structure	Inferred relationship	Some	1
Olivopontocerebellar atrophy-deafness syndrome is characterized by infancy-onset olivopontocerebellar atrophy, sensorineural deafness and speech impairment. It has been described in less than 15 children. Most cases were sporadic, but autosomal recessive inheritance was suggested in three cases.	Finding site	False	Cerebellar structure	Inferred relationship	Some	4
A rare, genetic form of pontocerebellar hypoplasia characterized by pontocerebellar hypoplasia and progressive neocortical atrophy that manifests clinically with uncoordinated sucking and swallowing, and generalized clonus in the neonate. In early childhood, spasticity, chorea/dyskinesia, seizures and progressive microcephaly develop. Voluntary motor development is lacking.	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
A rare autosomal recessive cerebellar ataxia, characterized by progressive cerebellar ataxia associated with oculomotor apraxia, severe neuropathy, and hypoalbuminemia.	Finding site	True	Cerebellar structure	Inferred relationship	Some	1
Spinocerebellar ataxia type 28 (SCA28) is a very rare subtype of type I autosomal dominant cerebellar ataxia. It is characterized by juvenile onset, slowly progressive cerebellar ataxia due to Purkinje cell degeneration.	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
An autosomal dominant cerebellar ataxia type I that is characterized by very slowly progressive or non-progressive ataxia, dysarthria, oculomotor abnormalities and intellectual disability.	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
An autosomal dominant cerebellar ataxia type III that is characterized by the late onset of ataxia, dysarthria and horizontal gaze nystagmus, and that is occasionally accompanied by pyramidal signs, tremor, decreased vibration sense and hearing difficulties.	Finding site	False	Cerebellar structure	Inferred relationship	Some	3
A very rare autosomal recessive, slowly progressive neurodegenerative disorder characterized by the triad of cerebellar ataxia (that generally manifests at adolescence or early adulthood), chorioretinal dystrophy, which may have a later onset (up to the fifth-sixth decade) leading to variable degrees of visual impairment, and hypogonadotropic hypogonadism (delayed puberty and lack of secondary sex characteristics). Ataxia-hypogonadism-choroidal dystrophy syndrome belongs to a clinical continuum of neurodegenerative disorders along with the clinically overlapping cerebellar ataxia-hypogonadism syndrome.	Finding site	False	Cerebellar structure	Inferred relationship	Some

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

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Id	Description	Lang	Type	Status	Case?	Module
187142017	Cerebellum	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
382977010	Cerebellar structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
648477018	Cerebellar structure (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
196921000077116	structure cérébelleuse	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
871751000172111	cervelet	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
955431000172118	cerebellum	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
1008081000172119	structure du cervelet	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module