Chronic brain syndrome

Code	`78689005`
Semantic tag	disorder
Module	international
Definition	defined
Effective time	20020131

785302009Adult-onset autosomal recessive cerebellar ataxia disorder

1299152003Adult-onset progressive leucoencephalopathy, early-onset deafness disorder

1259123006Amyotrophic lateral sclerosis, parkinsonism, dementia complex of Kii Peninsula disorder

1259121008Amyotrophic lateral sclerosis, parkinsonism, dementia complex of West New Guinea disorder

722964001Atypical Parkinsonism disorder

1237625002Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency disorder

773498006Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency disorder

783060009Autosomal recessive cerebellar ataxia, psychomotor delay syndrome disorder

45814002Birnbaum's syndrome disorder

715984007Boucher Neuhäuser syndrome disorder

1236804009Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome disorder

1217230002Cerebellar ataxia with oculomotor apraxia type 4 disorder

785301002Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia disorder

1172584005Childhood-onset basal ganglia degeneration syndrome disorder

1167373005Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder disorder

17258002Chronic anoxic encephalopathy disorder

1197758001Chronic bilirubin encephalopathy disorder

15139001Chronic brain-hydrocephalus syndrome disorder

230473009Chronic cluster headache disorder

124171000119105Chronic intractable migraine without aura disorder

27195007Chronic non-psychotic brain syndrome disorder

425919003Chronic organic mental disorder disorder

3456001Chronic progressive non-hereditary chorea disorder

230179001Chronic viral encephalitis disorder

783176002Congenital muscular dystrophy with cerebellar involvement disorder

783174004Congenital muscular dystrophy with intellectual disability disorder

782772000Congenital muscular dystrophy with intellectual disability and severe epilepsy disorder

1300192007Congenital pontocerebellar hypoplasia type 14 disorder

18842008Corticobasal degeneration disorder

1230018005Corticobasal syndrome disorder

783179009Cranio-cervical dystonia with laryngeal and upper limb involvement disorder

1281844004Dystonia 28 disorder

1222661007Early-onset calcifying leucoencephalopathy, skeletal dysplasia disorder

1169356004Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome disorder

1172588008Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome disorder

771469002Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome disorder

254132000Endosteal hyperostoses with cerebellar hypoplasia disorder

1208478005Familial infantile bilateral striatal necrosis disorder

774206008Fatal post-viral neurodegenerative disorder disorder

10394003Friedreich ataxia disorder

782690007Gemignani syndrome disorder

1172696009Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome disorder

45639009Hereditary cerebral amyloid angiopathy, Icelandic type disorder

770939009Huntington disease-like 3 disorder

721846006Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome disorder

1303273003IRF2BPL-related regressive neurodevelopmental disorder, dystonia, seizures syndrome disorder

1208747005ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement disorder

770725000Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly disorder

724226009Infantile osteopetrosis with neuroaxonal dysplasia syndrome disorder

1236805005MEPAN syndrome disorder

766246000Marburg acute multiple sclerosis disorder

720010009Microphthalmia with brain atrophy syndrome disorder

718214007Mitochondrial neurogastrointestinal encephalomyopathy syndrome disorder

1279891002Multiple mitochondrial dysfunctions syndrome type 6 disorder

192926004Multiple sclerosis of the brainstem disorder

785298001Muscle eye brain disease with bilateral multicystic leukodystrophy disorder

230426003Myoclonic epilepsy with ragged red fibres disorder

42012007Neuronal ceroid lipofuscinosis disorder

230279005Non-Alzheimer's progressive dysphasia disorder

722064003Odontoleukodystrophy disorder

1217367007PLAA-associated neurodevelopmental disorder disorder

1303280001PUM1-related cerebellar ataxia disorder

1237421000PYCR2-related microcephaly, progressive leucoencephalopathy disorder

49049000Parkinson's disease disorder

72585000Parkinsonian syndrome with idiopathic orthostatic hypotension disorder

24473007Persistent vegetative state disorder

1173997008Pontine autosomal dominant microangiopathy with leucoencephalopathy disorder

85039006Postpartum amenorrhoea-galactorrhea syndrome disorder

230278002Progressive aphasia disorder

1237413006Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome disorder

230246005Progressive bulbar palsy of childhood disorder

230240004Progressive cerebellar ataxia with hypogonadism disorder

1208481000Progressive cerebello-cerebral atrophy disorder

302811004Progressive congenital rubella encephalomyelitis disorder

442511009Progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy syndrome disorder

770678005Progressive encephalopathy with oedema, hypsarrhythmia, and optic atrophy-like syndrome disorder

764733009Progressive external ophthalmoplegia, myopathy, emaciation syndrome disorder

737228009Progressive focal cortical atrophy disorder

1172900005Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome disorder

783064000Progressive myoclonic epilepsy type 3 disorder

783055005Progressive myoclonic epilepsy type 5 disorder

783062001Progressive myoclonic epilepsy type 6 disorder

1208939001Progressive myoclonic epilepsy type 7 disorder

783139000Progressive myoclonic epilepsy type 8 disorder

1228857005Progressive myoclonic epilepsy type 9 disorder

771305006Progressive polyneuropathy with bilateral striatal necrosis disorder

359629000Progressive post haemorrhagic ventricular dilatation disorder

192976002Progressive supranuclear palsy disorder

783787000Retinal vasculopathy with cerebral leucoencephalopathy and systemic manifestations disorder

68618008Rett syndrome disorder

1208341008Severe oculo-renal-cerebellar syndrome disorder

1187278006Spastic paraplegia, severe developmental delay, epilepsy syndrome disorder

703524005Spinal muscular atrophy with progressive myoclonic epilepsy disorder

723612001Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome disorder

1208512000Spinocerebellar ataxia type 41 disorder

1208513005Spinocerebellar ataxia type 42 disorder

1208516002Spinocerebellar ataxia type 43 disorder

1279840000Spinocerebellar ataxia type 45 disorder

1279839002Spinocerebellar ataxia type 46 disorder

359686005Van Bogaert's sclerosing leucoencephalitis disorder

111504002Walker-Warburg congenital muscular dystrophy disorder

827172005X-linked progressive cerebellar ataxia disorder

Synonyms

Parents (2)

Children (102)