Adrenal insufficiency

Symptom Information:

Symptom ID: HPO:0000846
Synonyms:
Hypoadrenalism [HPO:0000846]
Adrenocortical insufficiency [Orphanet:41420]
Adrenal cortical hypofunction [Orphanet:41420]
Adrenal insufficiency [OMIM:Adrenal insufficiency]
Hypoadrenalism [OMIM:Hypoadrenalism]
Cortico-adrenal hypoplasia/insufficiency [Orphanet:41420]
Adrenal insufficiency (Addison disease) [OMIM:Adrenal insufficiency (Addison disease)]
Adrenocortical insufficiency (uncommon) [OMIM:Adrenocortical insufficiency (uncommon)]
Adrenal cortical hypofunctions [MedDRA:10001343]
Adrenal insufficiency [MedDRA:10001367]
Quality:
Cross references:
HPO:0008207 "Primary adrenal insufficiency" [Orphanet:41420]
HPO:0008182 "Adrenocortical hypoplasia" [Orphanet:41420]
HPO:0011735 "Adrenocorticotropin (ACTH) deficient adrenal insufficiency" [Orphanet:41420]
HPO:0000835 "Adrenal hypoplasia" [Orphanet:41420]
Orphanet:41420 "Cortico-adrenal hypoplasia/insufficiency" [Orphanet:41420]
OMIM: "Adrenal insufficiency" [OMIM:Adrenal insufficiency]
OMIM: "Hypoadrenalism" [OMIM:Hypoadrenalism]
OMIM: "Adrenal insufficiency (Addison disease)" [OMIM:Adrenal insufficiency (Addison disease)]
OMIM: "Adrenocortical insufficiency (uncommon)" [OMIM:Adrenocortical insufficiency (uncommon)]
UMLS:C0405580 "Adrenal cortical hypofunction" [Orphanet:41420]
Is a (Direct Parents):
MedDRA Adrenal gland disorders
Orphanet Abnormality of the adrenal glands
HPO         Abnormality of adrenal physiology
MedDRA Metabolic disorders NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the endocrine system(HPO:0000818)
          Abnormality of the adrenal glands(HPO:0000834)
             Abnormality of adrenal physiology(HPO:0011733)
                Adrenal insufficiency(HPO:0000846)
MedDRA:
Endocrine disorders(MedDRA:10014698)
    Adrenal gland disorders(MedDRA:10001353)
       Adrenal insufficiency(HPO:0000846)
Metabolism and nutrition disorders(MedDRA:10027433)
    Metabolism disorders NEC(MedDRA:10000546)
       Metabolic disorders NEC(MedDRA:10027428)
          Adrenal insufficiency(HPO:0000846)
Database Frequency: 24 / 7739
Resource:

All diseases associated with this symptom:

46,XY disorder of sex development - adrenal insufficiency due to CYP11A1 deficiency (Orphanet:168558)
ADRENAL HYPOPLASIA, CONGENITAL (OMIM:300200)
Addison disease (Orphanet:85138)
Adrenomyeloneuropathy (Orphanet:139399)
Autoimmune polyendocrinopathy type 1 (Orphanet:3453)
Bifunctional enzyme deficiency (Orphanet:300)
CORTICOTROPIN-RELEASING HORMONE (OMIM:122560)
Cytomegalic congenital adrenal hypoplasia (Orphanet:95702)
HYPOADRENOCORTICISM, FAMILIAL (OMIM:240200)
Immunodeficiency with natural-killer cell deficiency (Orphanet:75391)
Isolated glycerol kinase deficiency (Orphanet:408)
Kearns-Sayre syndrome (Orphanet:480)
MELAS (Orphanet:550)
Neonatal adrenoleukodystrophy (Orphanet:44)
Neonatal hemochromatosis (Orphanet:446)
Obesity due to pro-opiomelanocortin deficiency (Orphanet:71526)
Oculofaciocardiodental syndrome (Orphanet:2712)
PEROXISOME BIOGENESIS DISORDER 2B (OMIM:202370)
PITUITARY HORMONE DEFICIENCY, COMBINED, 2 (OMIM:262600)
Panhypopituitarism (Orphanet:90695)
Pearson syndrome (Orphanet:699)
Prader-Willi syndrome (Orphanet:739)
Short stature - pituitary and cerebellar defects - small sella turcica (Orphanet:85442)
X-linked cerebral adrenoleukodystrophy (Orphanet:139396)