Primary adrenocortical insufficiency

Preferred Label : Primary adrenocortical insufficiency;

Inclusion CIM-10 : Addison's disease; Autoimmune adrenalitis;

ICD-10 exclusion note : Addison only phenotype adrenoleukodystrophy (E71.528); Waterhouse-Friderichsen syndrome (A39.1); amyloidosis (E85.-); tuberculous Addison's disease (A18.7);

Diag associé à un acte (%) : 61.1;

Autres : 2;

CMA : 2;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

E271;

UMLS CUI

C0001403;

Automatic exact mappings (from CISMeF team)
- Addison's disease due to autoimmunity (disorder) [SNOMED CT concept]
- Autoimmune Primary Adrenal Insufficiency [NCIt concept]
- Autoimmune adrenalitis [MedDRA LLT]
Currated CISMeF NLP mapping
- ADDISON'S DISEASE [WHO-ART Included Term]
- Acquired adrenocortical insufficiency [ICD-11 Subcategory]
- Addison disease [ORDO Disease]
- Addison disease [PASCAL descriptor]
- Addison's Disease [NCIt concept]
- Addison's disease [MedDRA Preferred Term]
- Addison's disease [DO Concept]
- Addison's disease (disorder) [SNOMED CT concept]
- Disease Addison's [MedDRA LLT]
- Hypoadrenocorticism, familial [OMIM Phenotype]
- Primary adrenal insufficiency [HPO term]
- Primary adrenal insufficiency [MedDRA Preferred Term]
- Primary adrenocortical insufficiency (disorder) [SNOMED CT concept]
- addison disease [MeSH Descriptor]
- addison disease [MedlinePlus Topic]
- addison disease [MeSH concept]
- addison's disease, nos [SNOMED Notion]
DO Cross reference
- Addison's disease [DO Concept]
ICD-10 exclusion(s)
- Amyloidosis [ICD-10 category]
- Tuberculosis of adrenal glands [ICD-10 Sub-category]
- Waterhouse-Friderichsen syndrome [ICD-10 Sub-category]
Orphanet concepts
- Addison disease [ORDO Disease]
- Congenital adrenal hypoplasia of maternal cause [ORDO Disease]
- Familial adrenal hypoplasia with absent pituitary luteinizing hormone [ORDO Disease]
- Familial glucocorticoid deficiency [ORDO Disease]
- Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency [ORDO Disease]
- X-linked adrenal hypoplasia congenita [ORDO Disease]
See also inter- (CISMeF)
- Addison disease [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- ADDISON'S DISEASE [WHO-ART Included Term]
- Addison disease [HPO term]
- Addison disease [ORDO Disease]
- Addison disease [Disease (Nov.)]
- Addison's Disease [NCIt concept]
- Addison's disease [MedDRA Preferred Term]
- Addison's disease [DO Concept]
- Addison's disease (disorder) [SNOMED CT concept]
- Chronic adrenal insufficiency [HPO term]
- Chronic primary adrenal insufficiency [ORDO Disease]
- Disease Addison's [MedDRA LLT]
- Primary adrenal insufficiency [MedDRA Preferred Term]
- Primary adrenal insufficiency [HPO term]
- Primary adrenal insufficiency [ORDO Disease]
- Primary adrenocortical insufficiency [MedDRA LLT]
- Primary adrenocortical insufficiency (disorder) [SNOMED CT concept]
- Primary hypoadrenalism [MedDRA LLT]
- addison disease [MedlinePlus Topic]
- addison disease [MeSH Descriptor]
- addison disease [MeSH concept]
- addison's disease, nos [SNOMED Notion]

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