Concept information
Preferred term
Hereditary degenerative disease of central nervous system
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- Alexander's disease
- Amyotrophic lateral sclerosis type 4
- Autosomal dominant late onset Parkinson disease (disorder)
- Autosomal dominant striatal neurodegeneration (disorder)
- Autosomal recessive cerebral atrophy
- Autosomal recessive spastic ataxia type 4
- Behavioral variant of frontotemporal dementia (disorder)
- Brain calcification Rajab type (disorder)
- Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder)
- Cerebro-cutaneous syndrome with iron overload
- Coats plus syndrome
- Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome
- Craniosynostosis and intracranial calcification syndrome (disorder)
- Dermatoleukodystrophy
- Early onset parkinsonism and intellectual disability syndrome (disorder)
- Early-onset prion disease with prominent psychiatric features
- Encephalopathy, intracerebral calcification, retinal degeneration syndrome (disorder)
- Facial onset sensory and motor neuronopathy syndrome (disorder)
- Familial Alzheimer-like prion disease (disorder)
- Familial Creutzfeldt-Jakob (disorder)
- Fatal post-viral neurodegenerative disorder
- Frontotemporal dementia with gene located on 3p11 (disorder)
- Galactosylceramide beta-galactosidase deficiency
- HBSL - hypomyelination, brain stem, spinal cord, leg spasticity
- Hereditary cerebellar degeneration
- Hereditary dysphasic disinhibition dementia
- Hereditary spastic paraplegia
- Huntington disease-like syndrome due to chromosome 9 open reading frame 72 expansions (disorder)
- Huntington's chorea
- IHPRF (infantile hypotonia, psychomotor retardation, characteristic facies )syndrome
- Infantile choroidocerebral calcification syndrome (disorder)
- Keratosis follicularis, dwarfism, cerebral atrophy syndrome
- Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation
- Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder)
- Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome
- Microphthalmia with brain atrophy syndrome (disorder)
- Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome
- Muscle eye brain disease with bilateral multicystic leucodystrophy
- Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency (disorder)
- PEHO-like syndrome
- Pelizaeus Merzbacher like disease (disorder)
- Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease (disorder)
- Prion protein systemic amyloidosis (disorder)
- Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome
- Progressive myoclonic epilepsy due to KCTD7 deficiency
- Protein kinase cAMP-dependent type I regulatory subunit beta-related neurodegenerative dementia with intermediate filaments
- Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome (disorder)
- RNA polymerase III-related leukodystrophy
- Roifman Chitayat syndrome
- Severe X-linked intellectual disability Gustavson type (disorder)
- Severe X-linked mitochondrial encephalomyopathy (disorder)
- Spinocerebellar ataxia, amyotrophy, deafness syndrome
- Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome (disorder)
- Wilson's disease
- X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder)
Associated morphology
Finding site
Is a
In other languages
URI
http://www.irandoc.acir/onto/irandoc/106018006
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