keyboard_backspaceChronic brain syndrome

Domain IDCondition
Concept Class IDDisorder
Vocabulary ID
SNOMED
help_outline
Systematic Nomenclature of Medicine - Clinical Terms (IHTSDO)
2024-08-01 SNOMED CT International Edition; 2024-09-01 SNOMED CT US Edition; 2024-09-25 SNOMED CT UK Edition
http://www.nlm.nih.gov/research/umls/licensedcontent/umlsknowledgesources.html
Concept ID4301371
Concept code78689005
ValidityValid
ConceptStandard

Language	Synonym Concept
English	Chronic brain syndrome (disorder)
English	Chronic encephalopathy
Spanish	encefalopatía crónica
Spanish	síndrome cerebral crónico
Spanish	síndrome cerebral crónico (trastorno)

Valid start31-Jan-2002
Valid end31-Dec-2099

Term connections (124)

Relationship	Relates to	Concept id	Vocabulary
Has Module	SNOMED CT core	40642539	SNOMED
Has clinical course (SNOMED)	Chronic	4236661	SNOMED
Has finding site (SNOMED)	Brain structure	4133034	SNOMED
Has status	Defined	40642537	SNOMED
Is a	Chronic nervous system disorder	4134145	SNOMED
	Disorder of brain	372887	SNOMED
	Non-specific brain syndrome	378745	SNOMED
Non-standard to Standard map (OMOP)	Chronic brain syndrome	4301371	SNOMED
SNOMED to Indication/Contra-indication	Brain Damage, Chronic	4342030	NDFRT
Standard to Non-standard map (OMOP)	Brain Damage, Chronic	45617711	MeSH
	Chronic Brain Syndrome	45926959	CIEL
	Chronic brain syndrome	4301371	SNOMED
	Chronic encephalopathy	3361988	Nebraska Lexicon
	Encephalopathy Chronic	45913853	CIEL
	SYNDROME BRAIN CHRONIC	45529892	OXMIS
Subsumes	ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis	37312166	SNOMED
	Adult-onset autosomal recessive cerebellar ataxia	37205772	SNOMED
	Adult-onset progressive leukoencephalopathy, early-onset deafness	1245327	SNOMED
	Amyotrophic lateral sclerosis, parkinsonism, dementia complex of Kii Peninsula	37166121	SNOMED
	Amyotrophic lateral sclerosis, parkinsonism, dementia complex of West New Guinea	37166119	SNOMED
	Atypical Parkinsonism	36716783	SNOMED
	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency	37165112	SNOMED
	Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency	36676588	SNOMED
	Autosomal recessive cerebellar ataxia, psychomotor delay syndrome	37203830	SNOMED
	Birnbaum's syndrome	4164139	SNOMED
	Boucher Neuhäuser syndrome	37399488	SNOMED
	Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome	37164876	SNOMED
	Cerebellar ataxia with oculomotor apraxia type 4	37163549	SNOMED
	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia	37205771	SNOMED
	Childhood-onset basal ganglia degeneration syndrome	37160930	SNOMED
	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder	37160881	SNOMED
	Chronic bilirubin encephalopathy	37162909	SNOMED
	Chronic brain-hydrocephalus syndrome	4035481	SNOMED
	Chronic cerebrovascular accident	765568	SNOMED
	Chronic cluster headache	378145	SNOMED
	Chronic hypoxic-ischemic brain injury	762586	SNOMED
	Chronic intractable migraine without aura	43530652	SNOMED
	Chronic migraine without aura, non-refractory	765701	SNOMED
	Chronic non-psychotic brain syndrome	4099318	SNOMED
	Chronic organic mental disorder	4144146	SNOMED
	Chronic progressive epilepsia partialis continua	4219724	SNOMED
	Chronic progressive non-hereditary chorea	4144683	SNOMED
	Chronic viral encephalitis	4047623	SNOMED
	Chronic viral hepatitis C with hepatic coma	763021	SNOMED
	Congenital muscular dystrophy with cerebellar involvement	37204506	SNOMED
	Congenital muscular dystrophy with intellectual disability	37204504	SNOMED
	Congenital muscular dystrophy with intellectual disability and severe epilepsy	37204238	SNOMED
	Congenital pontocerebellar hypoplasia type 14	1245374	SNOMED
	Corticobasal degeneration	4077904	SNOMED
	Corticobasal syndrome	37164298	SNOMED
	Cranio-cervical dystonia with laryngeal and upper limb involvement	37204509	SNOMED
	Dystonia 28	37168488	SNOMED
	Early-onset calcifying leukoencephalopathy, skeletal dysplasia	37163908	SNOMED
	Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome	37160886	SNOMED
	Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome	37160933	SNOMED
	Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome	36675141	SNOMED
	Endosteal hyperostoses with cerebellar hypoplasia	4113736	SNOMED
	Familial infantile bilateral striatal necrosis	37163190	SNOMED
	Fatal post-viral neurodegenerative disorder	36676900	SNOMED
	Friedreich ataxia	441554	SNOMED
	Gemignani syndrome	37204181	SNOMED
	Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome	37160979	SNOMED
	Granulomatous meningoencephalitis	42599865	SNOMED Veterinary
	Hereditary cerebral amyloid angiopathy, Icelandic type	4164289	SNOMED
	Huntington disease-like 3	36674942	SNOMED
	Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome	36717190	SNOMED
	IRF2BPL-related regressive neurodevelopmental disorder, dystonia, seizures syndrome	1245413	SNOMED
	ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement	37163232	SNOMED
	Idiopathic feline polioencephalomyelitis	42599239	SNOMED Veterinary
	Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly	36674869	SNOMED
	Infantile osteopetrosis with neuroaxonal dysplasia syndrome	37119061	SNOMED
	Intermittently raised pressure hydrocephalus	4045838	SNOMED
	MEPAN syndrome	37164877	SNOMED
	Microphthalmia with brain atrophy syndrome	36714682	SNOMED
	Mitochondrial neurogastrointestinal encephalomyopathy syndrome	37397550	SNOMED
	Multiple mitochondrial dysfunctions syndrome type 6	37168390	SNOMED
	Muscle eye brain disease with bilateral multicystic leukodystrophy	37203915	SNOMED
	Myoclonic epilepsy with ragged red fibers	4044227	SNOMED
	Non-Alzheimer's progressive dysphasia	4046085	SNOMED
	Odontoleukodystrophy	36716159	SNOMED
	PLAA-associated neurodevelopmental disorder	37163583	SNOMED
	PUM1-related cerebellar ataxia	1245414	SNOMED
	PYCR2-related microcephaly, progressive leukoencephalopathy	37165069	SNOMED
	Parkinson's disease	381270	SNOMED
	Parkinsonian syndrome with idiopathic orthostatic hypotension	4219273	SNOMED
	Paroxysmal choreoathetosis	4172588	SNOMED
	Paroxysmal dystonia	4043386	SNOMED
	Persistent vegetative state	381686	SNOMED
	Pontine autosomal dominant microangiopathy with leukoencephalopathy	37161067	SNOMED
	Postpartum amenorrhea-galactorrhea syndrome	4225411	SNOMED
	Progressive aphasia	4046084	SNOMED
	Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome	37165065	SNOMED
	Progressive bulbar palsy of childhood	4043912	SNOMED
	Progressive cerebellar ataxia with hypogonadism	4047735	SNOMED
	Progressive cerebello-cerebral atrophy	37163193	SNOMED
	Progressive congenital rubella encephalomyelitis	4120303	SNOMED
	Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome	40483619	SNOMED
	Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome	36674825	SNOMED
	Progressive external ophthalmoplegia, myopathy, emaciation syndrome	35608088	SNOMED
	Progressive focal cortical atrophy	42537694	SNOMED
	Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome	37161029	SNOMED
	Progressive myoclonic epilepsy type 3	37204409	SNOMED
	Progressive myoclonic epilepsy type 5	37204403	SNOMED
	Progressive myoclonic epilepsy type 6	37203831	SNOMED
	Progressive myoclonic epilepsy type 7	37163334	SNOMED
	Progressive myoclonic epilepsy type 8	37204476	SNOMED
	Progressive myoclonic epilepsy type 9	37164081	SNOMED
	Progressive polyneuropathy with bilateral striatal necrosis	36675041	SNOMED
	Progressive post hemorrhagic ventricular dilatation	4230252	SNOMED
	Progressive supranuclear palsy	40391011	SNOMED
	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations	37204863	SNOMED
	Rett syndrome	4288480	SNOMED
	Severe oculo-renal-cerebellar syndrome	37163149	SNOMED
	Spastic paraplegia, severe developmental delay, epilepsy syndrome	37162298	SNOMED
	Spinal muscular atrophy with progressive myoclonic epilepsy	45766380	SNOMED
	Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome	37117168	SNOMED
	Spinocerebellar ataxia type 41	37163199	SNOMED
	Spinocerebellar ataxia type 42	37163200	SNOMED
	Spinocerebellar ataxia type 43	37163203	SNOMED
	Spinocerebellar ataxia type 45	37168353	SNOMED
	Spinocerebellar ataxia type 46	37168352	SNOMED
	Van Bogaert's sclerosing leukoencephalitis	4233538	SNOMED
	Walker-Warburg congenital muscular dystrophy	4009773	SNOMED
	X-linked progressive cerebellar ataxia	37311073	SNOMED

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Details

Term connections (124)

Athena – OHDSI Vocabularies Repository

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