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87536007: Central nervous system complication (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
145124010 Central nervous system complication en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
830030016 Central nervous system complication (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
125331000077118 complication liée au système nerveux central fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
2389611000195115 Komplikation des zentralen Nervensystems de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

846 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Central nervous system complication Is a Disorder of the central nervous system (disorder) true Inferred relationship Some
Central nervous system complication Is a complication false Inferred relationship Some
Central nervous system complication Finding site Structure of central nervous system (body structure) true Inferred relationship Some 1
Central nervous system complication Associated with Disease true Inferred relationship Some 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Cerebral infarction due to embolism of middle cerebral artery Is a True Central nervous system complication Inferred relationship Some
Cerebral infarction due to cerebral venous thrombosis, non-pyogenic Is a True Central nervous system complication Inferred relationship Some
Disorder due to and following injury of thoracic spinal cord (disorder) Is a True Central nervous system complication Inferred relationship Some
Arteritic anterior ischemic optic neuropathy due to giant cell arteritis (disorder) Is a True Central nervous system complication Inferred relationship Some
Acute seizure due to infection of central nervous system (disorder) Is a True Central nervous system complication Inferred relationship Some
Hydrocephalus due to Dandy-Walker malformation (disorder) Is a True Central nervous system complication Inferred relationship Some
Epilepsy due to scarring of brain (disorder) Is a True Central nervous system complication Inferred relationship Some
Cerebral infarction due to embolism of cerebral arteries Is a True Central nervous system complication Inferred relationship Some
Hypertrophic pachymeningitis due to disorder of immune function Is a True Central nervous system complication Inferred relationship Some
Ex-vacuo hydrocephalus due to infection Is a True Central nervous system complication Inferred relationship Some
Hydrocephalus due to tuberculosis of brain (disorder) Is a True Central nervous system complication Inferred relationship Some
Intracranial hypotension due to cerebrospinal fluid fistula Is a True Central nervous system complication Inferred relationship Some
Encephalopathy due to COVID-19 Is a True Central nervous system complication Inferred relationship Some
Top of basilar syndrome Is a True Central nervous system complication Inferred relationship Some
Retrobulbar neuritis due to late syphilis (disorder) Is a True Central nervous system complication Inferred relationship Some
Pachymeningitis due to inflammatory disorder Is a True Central nervous system complication Inferred relationship Some
Pachymeningitis due to secondary malignant neoplastic disease (disorder) Is a True Central nervous system complication Inferred relationship Some
Optic atrophy due to late syphilis (disorder) Is a True Central nervous system complication Inferred relationship Some
Traumatic spinal subarachnoid hemorrhage Is a True Central nervous system complication Inferred relationship Some
Ischemic stroke (disorder) Is a True Central nervous system complication Inferred relationship Some
Post infectious grand mal epilepsy (disorder) Is a True Central nervous system complication Inferred relationship Some
Post-cerebrovascular accident epilepsy Is a True Central nervous system complication Inferred relationship Some
Posttraumatic porencephalic cyst of brain Is a True Central nervous system complication Inferred relationship Some
Benign intracranial hypertension due to hypervitaminosis A (disorder) Is a True Central nervous system complication Inferred relationship Some
Meningoencephalitis due to Blastomyces dermatitidis Is a True Central nervous system complication Inferred relationship Some
Postinflammatory optic atrophy Is a True Central nervous system complication Inferred relationship Some
Spastic spinal syphilitic paralysis Is a True Central nervous system complication Inferred relationship Some
Brain disorder resulting from a period of impaired oxygen delivery to the brain (disorder) Is a True Central nervous system complication Inferred relationship Some
Intraventricular haemorrhage of prematurity Is a True Central nervous system complication Inferred relationship Some
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome is a rare mitochondrial disease due to a defect in coenzyme Q10 biosynthesis that manifests with a broad spectrum of signs and symptoms which may include: neonatal lactic acidosis, global developmental delay, tonus disorder, seizures, reduced spontaneous movements, ventricular hypertrophy, bradycardia, renal tubular dysfunction with massive lactic acid excretion in urine, severe biochemical defect of respiratory chain complexes II/III when assayed together and deficiency of coenzyme Q10 in skeletal muscle. Cerebral and cerebellar atrophy can be seen on magnetic resonance imaging and multiple choroid plexus cysts and symmetrical hyperechoic signal alterations in basal ganglia have been observed on ultrasound. Is a True Central nervous system complication Inferred relationship Some
Deafness-encephaloneuropathy-obesity-valvulopathy syndrome is a rare mitochondrial disease with marked clinical variability typically characterized by encephalomyopathy, kidney disease (nephrotic syndrome), optic atrophy, early-onset deafness, pancytopenia, obesity, and cardiac disease (valvulopathy). Additionally, macrocephaly, intellectual disability, hyperlactatemia, elevated lactate/pyruvate ratio, insulin-dependent diabetes, livedo reticularis, liver dysfunction and seizures have also been associated. Is a True Central nervous system complication Inferred relationship Some
Hypermethioninemia encephalopathy due to adenosine kinase deficiency is a rare inborn error of metabolism disorder characterized by persistent hypermethioninemia with increased levels of S-adenosylmethionine and S-adenosylhomocysteine which manifests with encephalopathy, severe global developmental delay, mild to severe liver dysfunction, hypotonia and facial dysmorphism (most significant is frontal bossing, macrocephaly, hypertelorism and depressed nasal bridge). Epileptic seizures, hypoglycemia and/or cardiac defects (pulmonary stenosis, atrial and/or ventricular septal defect, coarctation of the aorta) may be associated. Clinical picture may range from neurological symptoms only to multi-organ involvement. Is a True Central nervous system complication Inferred relationship Some
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency is a rare inborn error of metabolism disorder characterized by early-onset, acute, encephalopathic episodes (frequently triggered by viral infections), associated with lactic acidosis and alpha-ketoglutaric aciduria, which typically manifest with variable degrees of ataxia, generalized developmental regression (which deteriorates with each episode) and dystonia. Other manifestations include spasticity, seizures, truncal hypotonia, limb hypertonia, brisk tendon reflexes and reversible coma. Is a True Central nervous system complication Inferred relationship Some
A rare neuroinflammatory disease characterized by the onset of ataxia, dysarthria and cerebral white matter changes which are triggered by viral infection. Episodic progressive neurodegeneration (manifesting with loss of motor and verbal skills, muscle weakness, further cerebral white matter degeneration and, eventually, death) is observed in the absence of hematopathology, cytokine overproduction, fever, hypertriglyceridemia, hypofibrinogenemia and hyperferritinemia. Is a True Central nervous system complication Inferred relationship Some
Kernicterus due to isoimmunization Is a True Central nervous system complication Inferred relationship Some
Pituitary dwarfism Is a True Central nervous system complication Inferred relationship Some
Periventricular hemorrhagic venous infarct (disorder) Is a True Central nervous system complication Inferred relationship Some
Cerebral ischemic stroke due to dissection of artery (disorder) Is a True Central nervous system complication Inferred relationship Some
Cerebral ischemic stroke due to subarachnoid hemorrhage Is a True Central nervous system complication Inferred relationship Some
Hypersomatotropic gigantism Is a True Central nervous system complication Inferred relationship Some
Woodhouse-Sakati syndrome is a multisystemic disorder characterized by hypogonadism, alopecia, diabetes mellitus, intellectual deficit and extrapyramidal signs with choreoathetoid movements and dystonia. Is a True Central nervous system complication Inferred relationship Some
Hypoglycaemic coma Is a True Central nervous system complication Inferred relationship Some
Optic neuropathy due to folate deficiency (disorder) Is a False Central nervous system complication Inferred relationship Some
Disease with characteristics of delayed motor development, hypotonia and progressive neurodegeneration. To date, it has been described in four boys. The syndrome is caused by mutations affecting the two alleles of the HIBCH gene, encoding 3-hydroxyisobutyryl-CoA hydrolase which is caused by homozygous or compound heterozygous mutation in the HIBCH gene on chromosome 2q32. Is a True Central nervous system complication Inferred relationship Some
Parkinsonism co-occurrent and due to acute infection (disorder) Is a True Central nervous system complication Inferred relationship Some
Parkinsonism following infection (disorder) Is a True Central nervous system complication Inferred relationship Some
Non-infective meningitis due to inflammatory disorder (disorder) Is a True Central nervous system complication Inferred relationship Some
Parkinsonism due to heredodegenerative disorder (disorder) Is a True Central nervous system complication Inferred relationship Some
Late-onset central hypoventilation co-occurrent and due to hypothalamic dysfunction (disorder) Is a True Central nervous system complication Inferred relationship Some
Epilepsy due to infectious disease of central nervous system (disorder) Is a True Central nervous system complication Inferred relationship Some
Encephalopathy due to nutritional deficiency (disorder) Is a True Central nervous system complication Inferred relationship Some
Perceptual disturbances co-occurrent and due to psychoactive substance withdrawal (disorder) Is a False Central nervous system complication Inferred relationship Some
Parkinsonism due to and following injury of head (disorder) Is a True Central nervous system complication Inferred relationship Some
Chorea co-occurrent and due to Huntington disease-like condition (disorder) Is a True Central nervous system complication Inferred relationship Some
Chorea co-occurrent and due to Wilson disease (disorder) Is a False Central nervous system complication Inferred relationship Some
Ataxia co-occurrent and due to phytanic acid storage disease (disorder) Is a True Central nervous system complication Inferred relationship Some
White matter disorder co-occurrent and due to cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder) Is a True Central nervous system complication Inferred relationship Some
Demyelination of central nervous system co-occurrent and due to neurosarcoidosis (disorder) Is a True Central nervous system complication Inferred relationship Some
Demyelination of central nervous system co-occurrent and due to systemic lupus erythematosus (disorder) Is a True Central nervous system complication Inferred relationship Some
Demyelination of central nervous system co-occurrent and due to Sjogren disease (disorder) Is a False Central nervous system complication Inferred relationship Some
Demyelination of central nervous system co-occurrent and due to mitochondrial disease (disorder) Is a True Central nervous system complication Inferred relationship Some
Epilepsy due to perinatal anoxic-ischemic brain injury (disorder) Is a True Central nervous system complication Inferred relationship Some
Epilepsy due to cerebrovascular accident (disorder) Is a True Central nervous system complication Inferred relationship Some
Epilepsy due to intracranial neoplasm Is a True Central nervous system complication Inferred relationship Some
Autonomic nervous system disorder co-occurrent and due to neurodegenerative disorder (disorder) Is a True Central nervous system complication Inferred relationship Some
Epilepsy co-occurrent and due to degenerative brain disorder (disorder) Is a True Central nervous system complication Inferred relationship Some
Epilepsy co-occurrent and due to mesial temporal sclerosis (disorder) Is a True Central nervous system complication Inferred relationship Some
Epilepsy due to immune disorder (disorder) Is a True Central nervous system complication Inferred relationship Some
Epilepsy co-occurrent and due to demyelinating disorder (disorder) Is a True Central nervous system complication Inferred relationship Some
A rare, potentially fatal, epileptic encephalopathy characterized by explosive-onset of recurrent multifocal and bilateral tonic-clonic seizures following an unspecific febrile illness. The syndrome develops without a clear acute structural, toxic or metabolic cause, in a patient without previous epilepsy. FIRES is a subgroup of new-onset refractory status epilepticus (NORSE) and requires a preceding febrile infection as a mandatory feature. Is a True Central nervous system complication Inferred relationship Some
A rare pituitary deficiency characterized by herniation of the subarachnoid space into the sella turcica, resulting in flattening of the pituitary gland and endocrine dysfunction. Most common endocrine abnormalities are hyperprolactinemia and growth hormone deficit. Clinical symptoms are highly variable and include headaches, irregular menstruation, galactorrhea, obesity, and visual disturbances, among others. Is a True Central nervous system complication Inferred relationship Some
Encephalopathy due to sulfite oxidase deficiency is a rare neurometabolic disorder characterized by seizures, progressive encephalopathy and lens dislocation. Is a True Central nervous system complication Inferred relationship Some
Cerebrovascular accident due to right carotid artery occlusion Is a True Central nervous system complication Inferred relationship Some
Cerebrovascular accident due to right carotid artery stenosis Is a True Central nervous system complication Inferred relationship Some
Cerebrovascular accident due to left carotid artery stenosis Is a True Central nervous system complication Inferred relationship Some
Amnestic disorder associated with general medical condition (disorder) Is a True Central nervous system complication Inferred relationship Some
CVA - cerebrovascular accident due to cerebral artery occlusion Is a True Central nervous system complication Inferred relationship Some
Hydrocephalus following traumatic injury (disorder) Is a True Central nervous system complication Inferred relationship Some
Seizure co-occurrent and due to drug withdrawal Is a False Central nervous system complication Inferred relationship Some
This disease is characterized by progressive cerebellar ataxia with pyramidal and spinal cord dysfunction, associated with distinctive MRI anomalies and increased lactate in the abnormal white matter. Is a True Central nervous system complication Inferred relationship Some
Cupping of optic disc due to open angle glaucoma Is a True Central nervous system complication Inferred relationship Some
Secondary psychotic syndrome with hallucinations and delusions Is a False Central nervous system complication Inferred relationship Some
Disorder of central nervous system co-occurrent and due to infection with influenza virus (disorder) Is a True Central nervous system complication Inferred relationship Some
Wolfram-like syndrome is a rare endocrine disease characterized by the triad of adult-onset diabetes mellitus, progressive hearing loss (usually presenting in the first decade of life and principally of low to moderate frequencies), and/or juvenile-onset optic atrophy. Psychiatric (i.e. anxiety, depression, hallucinations) and sleep disorders, the only neurologic abnormalities observed in this disease, have been reported in rare cases. Unlike Wolfram syndrome, patients with Wolfram-like syndrome do not report endocrine or cardiac findings. Is a True Central nervous system complication Inferred relationship Some
Hypertrophic pachymeningitis due to infection (disorder) Is a True Central nervous system complication Inferred relationship Some
Status migrainosus co-occurrent and due to migraine without aura (disorder) Is a True Central nervous system complication Inferred relationship Some
Cerebrovascular accident due to stenosis of right vertebral artery (disorder) Is a True Central nervous system complication Inferred relationship Some
Cerebrovascular accident due to stenosis of left vertebral artery (disorder) Is a True Central nervous system complication Inferred relationship Some
Cerebrovascular accident due to occlusion of right vertebral artery (disorder) Is a True Central nervous system complication Inferred relationship Some
Cerebrovascular accident due to occlusion of left vertebral artery (disorder) Is a True Central nervous system complication Inferred relationship Some
Lacunar ataxic hemiparesis of right dominant side Is a False Central nervous system complication Inferred relationship Some
Lacunar ataxic hemiparesis of left dominant side Is a False Central nervous system complication Inferred relationship Some
Lacunar ataxic hemiparesis of left nondominant side Is a False Central nervous system complication Inferred relationship Some
Lacunar ataxic hemiparesis of right nondominant side Is a False Central nervous system complication Inferred relationship Some
Cerebrovascular accident due to occlusion of left pontine artery (disorder) Is a True Central nervous system complication Inferred relationship Some
Cerebrovascular accident due to occlusion of right pontine artery (disorder) Is a True Central nervous system complication Inferred relationship Some
Cerebrovascular accident due to occlusion of left carotid artery (disorder) Is a True Central nervous system complication Inferred relationship Some
Cerebrovascular accident due to occlusion of left cerebellar artery (disorder) Is a True Central nervous system complication Inferred relationship Some
Cerebrovascular accident due to occlusion of right cerebellar artery (disorder) Is a True Central nervous system complication Inferred relationship Some
Tuberculous abscess of epidural space (disorder) Is a True Central nervous system complication Inferred relationship Some
A disorder characterized by a decline primarily in intellectual function due to disease of the brain caused by a variety of acquired conditions such as cerebrovascular disease, Alzheimer's disease, infections, adverse drug reactions and trauma. Is a True Central nervous system complication Inferred relationship Some

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