Degenerative brain disorder (disorder)
| Code | 52522001 |
|---|---|
| Semantic tag | disorder |
| Module | international |
| Definition | defined |
| Effective time | 20060131 |
80690008Degenerative disease of the central nervous system
disorder
81308009Disorder of brain
disorder
83942000Acute disseminated encephalomyelitis
disorder
4113009Arrested hydrocephalus
disorder
1144381008Atrophy of brainstem
disorder
1296731001Atypical Krabbe disease due to saposin A deficiency
disorder
6807001Central pontine myelinolysis
disorder
95646004Cerebellar degeneration
disorder
28634005Cerebral ataxia
disorder
418143002Cerebral degeneration
disorder
1167373005Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder
disorder
111033008Circumscribed atrophy of brain
disorder
1259630004Clinically isolated syndrome of brainstem
disorder
1172844009Combined oxidative phosphorylation defect type 27
disorder
445166009Cystic degeneration of brain
disorder
133301000119102Degenerative brain disorder caused by alcohol
disorder
1169356004Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome
disorder
724988000Epilepsy co-occurrent and due to degenerative brain disorder
disorder
230377009Extrapontine myelinolysis
disorder
774206008Fatal post-viral neurodegenerative disorder
disorder
774151000Ferro-cerebro-cutaneous syndrome
disorder
1144430004Global brain atrophy
disorder
763722004Hypotonia, speech impairment, severe cognitive delay syndrome
disorder
1303273003IRF2BPL-related regressive neurodevelopmental disorder, dystonia, seizures syndrome
disorder
724228005Infantile choroidocerebral calcification syndrome
disorder
29570005Leigh's disease
disorder
720010009Microphthalmia with brain atrophy syndrome
disorder
1279891002Multiple mitochondrial dysfunctions syndrome type 6
disorder
192926004Multiple sclerosis of the brainstem
disorder
1251447008NAD(P)HX epimerase deficiency
disorder
230365004Neuroaxonal dystrophy
disorder
722488009Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency
disorder
42012007Neuronal ceroid lipofuscinosis
disorder
774069007PRKAR1B-related neurodegenerative dementia with intermediate filaments
disorder
22381000119105Primary degenerative dementia
disorder
723124007Primary progressive apraxia of speech
disorder
20484008Prion disease
disorder
442511009Progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy syndrome
disorder
770678005Progressive encephalopathy with oedema, hypsarrhythmia, and optic atrophy-like syndrome
disorder
783064000Progressive myoclonic epilepsy type 3
disorder
1172698005Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome
disorder
716200002Schofer Beetz Bohl syndrome
disorder
45864009Senile degeneration of brain
disorder
722212004Severe X-linked mitochondrial encephalomyopathy
disorder
715504003Spastic paraparesis and deafness
disorder
1251449006USP18 deficiency
disorder
88518009Wilson's disease
disorder