Concept information
...
Disease of nervous system
Disease of the central nervous system
Degenerative disease of the central nervous system
Hereditary degenerative disease of central nervous system
...
disease
Degenerative disorder
Degenerative disease of the central nervous system
Hereditary degenerative disease of central nervous system
...
Genetic disease
Hereditary disease
Autosomal hereditary disorder
Dominant hereditary disorder, NOS
...
Congenital malformation
Congenital malformation syndrome (disorder)
Multiple system malformation syndrome
Waardenburg's syndrome
...
Congenital malformation
Congenital malformation syndrome (disorder)
Multiple system malformation syndrome
Waardenburg's syndrome
...
Skin lesion
Anomalous pigmentation of skin
Genetic disorder of skin pigmentation (disorder)
Waardenburg's syndrome
...
Skin lesion
Anomalous pigmentation of skin
Genetic disorder of skin pigmentation (disorder)
Waardenburg's syndrome
...
Skin lesion
Anomalous pigmentation of skin
Genetic disorder of skin pigmentation (disorder)
Waardenburg's syndrome
...
Disorder of pigmentation (disorder)
Anomalous pigmentation of skin
Genetic disorder of skin pigmentation (disorder)
Waardenburg's syndrome
Preferred term
Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease (disorder)
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Associated morphology
- 125495003
- Demyelination
- Dystrophy
- Hypopigmentation
Finding site
- 389080008
- 54115001
- Ear-related structure
- peripheral nerve
- skin
Interprets
Is a
Occurrence
Pathological process
In other languages
URI
http://www.irandoc.acir/onto/irandoc/765325002
{{label}}
{{#each values }} {{! loop through ConceptPropertyValue objects }}
{{#if prefLabel }}
{{/if}}
{{/each}}
{{#if notation }}{{ notation }} {{/if}}{{ prefLabel }}
{{#ifDifferentLabelLang lang }} ({{ lang }}){{/ifDifferentLabelLang}}
{{#if vocabName }}
{{ vocabName }}
{{/if}}

