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Orphanet Rare Disease Ontology
Last uploaded:
December 4, 2024
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| Preferred Name | Addison disease | |
| Synonyms |
Autoimmune adrenalitis Primary Addison disease Classic Addison disease Autoimmune Addison disease |
|
| Definitions |
A chronic and rare endocrine disorder due to autoimmune destruction of the adrenal cortex and resulting in a glucocorticoid and mineralocorticoid deficiency. Properly speaking, it designates autoimmune adrenalitis, but it is a term commonly used to describe any form of chronic primary adrenal insufficiency (CPAI). |
|
| ID |
http://www.orpha.net/ORDO/Orphanet_85138 |
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| alternative_term |
Autoimmune adrenalitis Primary Addison disease Classic Addison disease Autoimmune Addison disease
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|
| definition |
A chronic and rare endocrine disorder due to autoimmune destruction of the adrenal cortex and resulting in a glucocorticoid and mineralocorticoid deficiency. Properly speaking, it designates autoimmune adrenalitis, but it is a term commonly used to describe any form of chronic primary adrenal insufficiency (CPAI).
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| definition_citation |
Orphanet
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| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=85138 |
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| has_age_of_onset |
All ages
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| has_inheritance |
Not applicable
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| hasDbXref |
MeSH:D000224 OMIM:240200 OMIM:103230 ICD-10:E27.1 UMLS:C0001403 MedDRA:10001130 ICD-11:5A74.0
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|
| label |
Addison disease
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|
| notation |
ORPHA:85138
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| part_of | ||
| prefixIRI |
ORDO:Orphanet_85138
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|
| prefLabel |
Addison disease
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| present_in |
United Kingdom AND has_point_prevalence_average_value : 9.3 AND has_point_prevalence_range : 1-9 / 100 000 Europe AND has_point_prevalence_average_value : 12.5 AND has_point_prevalence_range : 1-5 / 10 000 Specific population AND has_annual_incidence_average_value : 54.0 AND has_annual_incidence_range : 1-5 / 10 000 Norway AND has_point_prevalence_average_value : 14.0 AND has_point_prevalence_range : 1-5 / 10 000
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| treeView | ||
| subClassOf |
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