Primary adrenal insufficiency

Symptom Information:

Symptom ID: HPO:0008207
Synonyms:
Addison disease [HPO:0008207]
Addison's disease [HPO:0008207]
Adrenocortical insufficiency [HPO:0008207]
Primary adrenocortical failure [HPO:0008207]
Adrenocortical insufficiency [Orphanet:41420]
Adrenal cortical hypofunction [Orphanet:41420]
Addison disease [OMIM:Addison disease]
Adrenocortical insufficiency [OMIM:Adrenocortical insufficiency]
Primary adrenal insufficiency [OMIM:Primary adrenal insufficiency]
Primary adrenocortical failure [OMIM:Primary adrenocortical failure]
Cortico-adrenal hypoplasia/insufficiency [Orphanet:41420]
Adrenocortical insufficiency (uncommon) [OMIM:Adrenocortical insufficiency (uncommon)]
Adrenal cortical hypofunctions [MedDRA:10001343]
Primary adrenal insufficiency [MedDRA:10052381]
Addison's disease [MedDRA:10001130]
Quality:
Cross references:
HPO:0008182 "Adrenocortical hypoplasia" [Orphanet:41420]
HPO:0011735 "Adrenocorticotropin (ACTH) deficient adrenal insufficiency" [Orphanet:41420]
HPO:0000835 "Adrenal hypoplasia" [Orphanet:41420]
HPO:0000846 "Adrenal insufficiency" [Orphanet:41420]
Orphanet:41420 "Cortico-adrenal hypoplasia/insufficiency" [Orphanet:41420]
OMIM: "Addison disease" [OMIM:Addison disease]
OMIM: "Adrenocortical insufficiency" [OMIM:Adrenocortical insufficiency]
OMIM: "Primary adrenal insufficiency" [OMIM:Primary adrenal insufficiency]
OMIM: "Primary adrenocortical failure" [OMIM:Primary adrenocortical failure]
OMIM: "Adrenocortical insufficiency (uncommon)" [OMIM:Adrenocortical insufficiency (uncommon)]
UMLS:C0405580 "Adrenal cortical hypofunction" [Orphanet:41420]
Is a (Direct Parents):
Orphanet Abnormality of the adrenal glands
HPO         Adrenal insufficiency
MedDRA Endocrine autoimmune disorders
MedDRA Adrenal gland disorders
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)
                   Primary adrenal insufficiency(HPO:0008207)
MedDRA:
Endocrine disorders(MedDRA:10014698)
    Adrenal gland disorders(MedDRA:10001353)
       Primary adrenal insufficiency(HPO:0008207)
Immune system disorders(MedDRA:10021428)
    Autoimmunity(HPO:0002960)
       Endocrine autoimmune disorders(MedDRA:10003818)
          Primary adrenal insufficiency(HPO:0008207)
Metabolism and nutrition disorders(MedDRA:10027433)
    Metabolism disorders NEC(MedDRA:10000546)
       Metabolic disorders NEC(MedDRA:10027428)
          Primary adrenal insufficiency(HPO:0008207)
Database Frequency: 26 / 7739
Resource:

All diseases associated with this symptom:

14q22q23 microdeletion syndrome (Orphanet:264200)
3C syndrome (Orphanet:7)
46,XY partial gonadal dysgenesis (Orphanet:251510)
8p23.1 microduplication syndrome (Orphanet:251076)
ADRENAL HYPOPLASIA, CONGENITAL (OMIM:300200)
ADRENAL HYPOPLASIA, CYTOMEGALIC TYPE (OMIM:202155)
Adrenomyodystrophy (Orphanet:977)
Autoimmune polyendocrinopathy type 1 (Orphanet:3453)
Autoimmune polyendocrinopathy type 2 (Orphanet:3143)
Beta-thalassemia major (Orphanet:231214)
Bifunctional enzyme deficiency (Orphanet:300)
Distal monosomy 13q (Orphanet:1590)
Flynn-Aird syndrome (Orphanet:2047)
Holoprosencephaly - postaxial polydactyly (Orphanet:2166)
Isolated anencephaly/exencephaly (Orphanet:1048)
Isolated glycerol kinase deficiency (Orphanet:408)
Kearns-Sayre syndrome (Orphanet:480)
MELAS (Orphanet:550)
Neonatal adrenoleukodystrophy (Orphanet:44)
Orofaciodigital syndrome type 4 (Orphanet:2753)
POEMS syndrome (Orphanet:2905)
Pallister-Hall syndrome (Orphanet:672)
Pituitary stalk interruption syndrome (Orphanet:95496)
Triple A syndrome (Orphanet:869)
X-linked cerebral adrenoleukodystrophy (Orphanet:139396)
Zellweger syndrome (Orphanet:912)