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loading...| Preferred Name |
Amyloidosis |
| ID |
http://www.orpha.net/ORDO/Orphanet_69 |
| definition |
A vast group of rare systemic diseases characterized by the presence of insoluble fibrillar protein deposits in tissues. Amyloidoses are classified according to biochemical type of amyloid protein involved. |
| definition_citation |
Orphanet |
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=69 |
| has_age_of_onset |
All ages |
| hasDbXref |
MeSH:D000686 UMLS:C0002726 ICD-10:E85.0 ICD-11:5D00 MedDRA:10002022 |
| label |
Amyloidosis |
| notation |
Category ORPHA:69 |
| prefixIRI |
ORDO:Orphanet_69 |
| prefLabel |
Amyloidosis |
| present_in |
Worldwide AND has_point_prevalence_range : Unknown Korea, Republic of AND has_point_prevalence_average_value : 1.91 AND has_point_prevalence_range : 1-9 / 100 000 |
| subClassOf |
http://www.orpha.net/ORDO/Orphanet_182222 |
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