Concept information
Preferred term
Inherited metabolic disorder of nervous system
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- Arginase deficiency
- Aspartylglucosaminuria
- Cerebral lipidosis
- Combined deficiency of sialidase AND beta galactosidase
- Deficiency of cerebroside-sulfatase
- Deficiency of monoamine oxidase A (disorder)
- Leber's optic atrophy
- Neonatal epileptic encephalopathy due to glutaminase deficiency
- Neuronal ceroid lipofuscinosis
- Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency
- Niemann-Pick disease, type A
- Niemann-Pick disease, type C, acute form
- Phytanic acid storage disease
- Subacute neuronopathic Gaucher's disease
- Thyrotoxicosis due to pituitary thyroid hormone resistance
Finding site
Occurrence
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/128190004
{{label}}
{{#each values }} {{! loop through ConceptPropertyValue objects }}
{{#if prefLabel }}
{{/if}}
{{/each}}
{{#if notation }}{{ notation }} {{/if}}{{ prefLabel }}
{{#ifDifferentLabelLang lang }} ({{ lang }}){{/ifDifferentLabelLang}}
{{#if vocabName }}
{{ vocabName }}
{{/if}}

