Degenerative brain disorder 52522001 SNOMED CT code SNOMED code 52522001 name Degenerative brain disorder status active date introduced 2002-01-31 fully specified name(s) Degenerative brain disorder (disorder) synonyms Degenerative brain disorder attributes - group1 Associated morphology Degenerative abnormality 107669003 Finding site Brain structure 12738006 parents Degenerative disease of the central nervous system 80690008 Disorder of brain 81308009 children Abortive cerebellar ataxia 66988006 removed: 2016-07-31 Acute disseminated encephalomyelitis 83942000 Arrested hydrocephalus 4113009 Atypical Krabbe disease due to saposin A deficiency 1296731001 Central pontine myelinolysis 6807001 Cerebellar degeneration 95646004 Cerebral ataxia 28634005 Cerebral degeneration 418143002 Cerebral degeneration in lipidoses EC 192790005 removed: 2006-01-31 Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder 1167373005 Circumscribed atrophy of brain 111033008 Clinically isolated syndrome of brainstem 1259630004 Combined oxidative phosphorylation defect type 27 1172844009 Cystic degeneration of brain 445166009 Degenerative brain disorder caused by alcohol 133301000119102 Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome 1169356004 Epilepsy co-occurrent and due to degenerative brain disorder 724988000 Extrapontine myelinolysis 230377009 Fatal post-viral neurodegenerative disorder 774206008 Ferro-cerebro-cutaneous syndrome 774151000 GRN-related frontotemporal dementia 702426001 Hereditary amblyopia with quadriplegia in the Irish Setter 34933004 removed: 2014-01-31 Hypotonia, speech impairment, severe cognitive delay syndrome 763722004 Infantile choroidocerebral calcification syndrome 724228005 ITM2B-related amyloidosis 1187126002 Kernicterus of newborn 50143004 Leigh's disease 29570005 Microphthalmia with brain atrophy syndrome 720010009 Multiple mitochondrial dysfunctions syndrome type 6 1279891002 Multiple sclerosis of the brainstem 192926004 NAD(P)HX epimerase deficiency 1251447008 Neuroaxonal dystrophy 230365004 Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency 722488009 Other cerebral degenerations 192801009 removed: 2010-01-31 Primary degenerative dementia 22381000119105 Primary progressive apraxia of speech 723124007 Prion disease 20484008 PRKAR1B-related neurodegenerative dementia with intermediate filaments 774069007 Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome 442511009 Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome 770678005 Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome 1172698005 Schofer Beetz Bohl syndrome 716200002 Senile brain amyloidosis 4645000 Senile degeneration of brain 45864009 Severe X-linked mitochondrial encephalomyopathy 722212004 Spastic paraparesis and deafness 715504003 USP18 deficiency 1251449006 Wilson's disease 88518009 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 64572001 362975008 80690008 52522001 138875005 404684003 246556002 299718000 81308009 52522001 ancestors sorted most to least specific
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