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370502006: Encephalomyelopathy (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1195795016 Encephalomyelopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1209236011 Encephalomyelopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1805081000195117 encefalomielopatia it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
276541000077111 encéphalomyélopathie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

128 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Encephalomyelopathy (disorder) Is a Disorder of brain (disorder) true Inferred relationship Some
Encephalomyelopathy (disorder) Is a Spinal cord disorder (disorder) true Inferred relationship Some
Encephalomyelopathy (disorder) Finding site Brain structure true Inferred relationship Some 1
Encephalomyelopathy (disorder) Finding site Spinal cord structure true Inferred relationship Some 2
Inbound Relationships Type Active Source Characteristic Refinability Group
paralysie paralytique infantile Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Acute paralytic non-bulbar poliomyelitis Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Vacuolar myelopathy Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Segmental cord myoclonus Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Painful legs and moving toes Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Traumatic spinal subarachnoid hemorrhage Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Traumatic spinal subdural hematoma Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Non-traumatic spinal subdural haematoma Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Acute nonparalytic poliomyelitis Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Spinopontine degeneration Is a True Encephalomyelopathy (disorder) Inferred relationship Some
Arnold-Chiari syndrome Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Meningoencephalomyelitis Is a True Encephalomyelopathy (disorder) Inferred relationship Some
Restless legs Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Hereditary spastic paraplegia Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Myelitis Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Human T-cell lymphotropic virus 1-associated myelopathy-tropical spastic paraparesis Is a False Encephalomyelopathy (disorder) Inferred relationship Some
A rare neurological disorder comprising fluctuating trunk and limb stiffness, painful muscle spasms, task-specific phobia related to walking, an exaggerated startle response, and often ankylosing deformities such as fixed lumbar hyperlordosis. Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Spina bifida with hydrocephalus Is a False Encephalomyelopathy (disorder) Inferred relationship Some
A disorder characterized by inflammation of both the brain and the spinal cord. Is a True Encephalomyelopathy (disorder) Inferred relationship Some
Metastatic malignant neoplasm to brain and spinal cord Is a True Encephalomyelopathy (disorder) Inferred relationship Some
Equine degenerative myeloencephalopathy Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Acute non-infective transverse myelitis Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Acute necrotizing myelitis Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Ependymal cyst Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Spinocerebellar disease Is a True Encephalomyelopathy (disorder) Inferred relationship Some
Spina bifida with hydrocephalus - closed Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Spina bifida with hydrocephalus of late onset Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Rachischisis with hydrocephalus Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Myelocele with hydrocephalus (disorder) Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Hydromyelocele with hydrocephalus Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Fissured spine with hydrocephalus Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Spina bifida with hydrocephalus - open Is a True Encephalomyelopathy (disorder) Inferred relationship Some
Perinatal subependymal haemorrhage Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Ependymitis Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Ependymal cyst of spinal cord (disorder) Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Syringomyelia and syringobulbia Is a True Encephalomyelopathy (disorder) Inferred relationship Some
Myelomeningocele co-occurrent with hydrocephalus (disorder) Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Encephalomyelocele Is a True Encephalomyelopathy (disorder) Inferred relationship Some
Injuries of brain and cranial nerves with injuries of nerves and spinal cord at neck level Is a True Encephalomyelopathy (disorder) Inferred relationship Some
Pyogranulomatous meningoencephalomyelitis Is a False Encephalomyelopathy (disorder) Inferred relationship Some
Spastic paraplegia-severe developmental delay-epilepsy syndrome is a rare, genetic, complex spastic paraplegia disorder characterized by an infantile-onset of psychomotor developmental delay with severe intellectual disability and poor speech acquisition, associated with seizures (mostly myoclonic), muscular hypotonia which may be noted at birth, and slowly progressive spasticity in the lower limbs leading to severe gait disturbances. Ocular abnormalities and incontinence are commonly associated. Other symptoms may include verbal dyspraxia, hypogenitalism, macrocephaly and sensorineural hearing loss, as well as dystonic movements and ataxia with upper limb involvement. Is a True Encephalomyelopathy (disorder) Inferred relationship Some
A rare neurometabolic disease characterized by infantile onset of rapidly progressive neurological deterioration, typically precipitated by a febrile illness. Patients present with hypotonia, loss of previously acquired motor milestones and cognitive skills, ataxia, nystagmus, tremor, seizures, tetraparesis, and respiratory failure, eventually resulting in a vegetative state. Imaging of the brain and spinal cord may show white matter abnormalities, cerebral atrophy, cerebellar edema, and spinal myelopathy. Subacute development of extensive bullous skin lesions within weeks of onset of neurological symptoms has also been reported. Is a True Encephalomyelopathy (disorder) Inferred relationship Some
CLIPPERS is a rare neuroinflammatory disorder characterized by brainstem-predominant encephalomyelitis which typically presents with cerebellar and cranial nerve manifestations (gait ataxia, dysarthria, visual disorders, parasthesias), as well as brainstem, myelopathy and cognitive findings, that respond to steroid treatment. Punctate curvilinear post-gadolinium contrast enhancement predominantly in the pons and cerebellum is observed on brain MRI and prominent, perivascular, CD3+ T-cell predominantly lymphocytic inflammation in neuropathology. Is a True Encephalomyelopathy (disorder) Inferred relationship Some

This concept is not in any reference sets

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