Concept information
...
Genetic disease
Hereditary disease
Autosomal hereditary disorder
Dominant hereditary disorder, NOS
Preferred term
Alpha-B crystallin-related late-onset myopathy
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Clinical course
Finding site
Is a
- 128237006
- 363212003
- Dominant hereditary disorder, NOS
- Myofibrillar myopathy
Occurrence
In other languages
URI
http://www.irandoc.acir/onto/irandoc/783770002
{{label}}
{{#each values }} {{! loop through ConceptPropertyValue objects }}
{{#if prefLabel }}
{{/if}}
{{/each}}
{{#if notation }}{{ notation }} {{/if}}{{ prefLabel }}
{{#ifDifferentLabelLang lang }} ({{ lang }}){{/ifDifferentLabelLang}}
{{#if vocabName }}
{{ vocabName }}
{{/if}}

