Concept information
Preferred term
Hereditary disorder of nervous system
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- Acute neuronopathic Gaucher's disease
- Aicardi's syndrome
- Amyotonia congenita
- Ataxia-telangiectasia syndrome
- Beckwith-Wiedemann syndrome
- Borjeson-Forssman-Lehmann syndrome
- Cerebral folate transport deficiency (disorder)
- Cockayne syndrome
- Congenital isolated adrenocorticotropic hormone deficiency (disorder)
- Familial hemiplegic migraine
- Familial isolated vitamin E deficiency
- Familial motor neuron disease
- Giant axonal neuropathy
- Hereditary degenerative disease of central nervous system
- Hereditary infantile gigantism
- Hereditary motor end-plate disease
- Hereditary nephrogenic diabetes insipidus
- Hereditary neuraxial edema
- Hypermanganesemia with dystonia (disorder)
- Inherited metabolic disorder of nervous system
- Kallman syndrome with heart disease (disorder)
- Lowe syndrome
- Menkes kinky-hair syndrome
- Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome (disorder)
- Neurofibromatosis, type 1
- Neurofibromatosis, type 2
- Neurologic xeroderma pigmentosum
- Peutz-Jeghers syndrome
- Primary CD59 deficiency
- Sotos' syndrome
- Von Hippel-Lindau syndrome
- X-linked spasticity, intellectual disability, epilepsy syndrome (disorder)
Finding site
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/363235000
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