Primary adrenal insufficiency
Symptom Information:
Symptom ID: | HPO:0008207 | |||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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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) Metabolism and nutrition disorders(MedDRA:10027433) Metabolism disorders NEC(MedDRA:10000546) Metabolic disorders NEC(MedDRA:10027428) Primary adrenal insufficiency(HPO:0008207) Immune system disorders(MedDRA:10021428) Autoimmunity(HPO:0002960) Endocrine autoimmune disorders(MedDRA:10003818) Primary adrenal insufficiency(HPO:0008207) |
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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) |