Concept information
Preferred term
Chronic brain syndrome
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- Adult-onset autosomal recessive cerebellar ataxia (disorder)
- AFG3L2 (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome
- ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis
- Autosomal recessive cerebellar ataxia, psychomotor delay syndrome (disorder)
- Autosomal recessive spinocerebellar ataxia type 7
- Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome (disorder)
- Congenital muscular dystrophy with cerebellar involvement
- Congenital muscular dystrophy with intellectual disability
- Congenital muscular dystrophy with intellectual disability and severe epilepsy
- Dystonia 24
- Fatal post-viral neurodegenerative disorder
- Frequent episodic tension-type headache (disorder)
- Hereditary cerebral amyloid angiopathy, Icelandic type
- Huntington disease-like 3
- Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder)
- Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
- Infantile osteopetrosis with neuroaxonal dysplasia syndrome (disorder)
- Mitochondrial neurogastrointestinal encephalomyopathy syndrome (disorder)
- Muscle eye brain disease with bilateral multicystic leucodystrophy
- Non-Alzheimer's progressive dysphasia
- Odontoleukodystrophy (disorder)
- Paroxysmal dystonia
- PEHO-like syndrome
- Persistent vegetative state
- Progressive aphasia
- Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome
- Progressive external ophthalmoplegia, myopathy, emaciation syndrome
- Progressive myoclonic epilepsy due to KCTD7 deficiency
- Progressive myoclonic epilepsy type 5 (disorder)
- Progressive myoclonic epilepsy type 6 (disorder)
- Progressive myoclonic epilepsy type 8 (disorder)
- Progressive polyneuropathy with bilateral striatal necrosis
- Progressive post haemorrhagic ventricular dilatation
- Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
- Rett's disorder
- Semantic dementia
- Spinocerebellar ataxia, amyotrophy, deafness syndrome
- Spinocerebellar ataxia autosomal recessive type 23
- Thoracic dysplasia and hydrocephalus syndrome
- X-linked progressive cerebellar ataxia
Clinical course
Finding site
Is a
- 128283000
- Disease of brain
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/78689005
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