Concept information
Preferred term
Hereditary disorder of nervous system
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- Autosomal dominant idiopathic familial dystonia
- Autosomal recessive idiopathic familial dystonia
- Benign hereditary chorea
- Benign neonatal epilepsy
- Cerebral folate transport deficiency (disorder)
- Choroid plexus carcinoma
- Endosteal hyperostoses with cerebellar hypoplasia
- Epilepsy telangiectasia syndrome (disorder)
- Familial congenital controlateral synkinesia
- Genetically determined myasthenia
- Hereditary degenerative disease of central nervous system
- Hereditary peripheral neuropathy
- Hypomagnesemia with secondary hypocalcemia (disorder)
- Joubert syndrome (disorder)
- Kohlschutter's syndrome
- MERRF - Myoclonic epilepsy - ragged red fibres
- Muscle-eye-brain disease, congenital muscular dystrophy
- Panhypopituitarism - X-linked
- Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction
- Tuberous sclerosis syndrome
- Walker-Warburg congenital muscular dystrophy
- XK aprosencephaly syndrome (disorder)
Finding site
Is a
- 363137000
- Disease of nervous system
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/363235000
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