MSeqDR Mitochondrial Disease Portal


 
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Parent Node:
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autoimmune disease (MONDO:0007179)
Parent Node:
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endocrine system disease (MONDO:0005151)
..Starting node
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autoimmune disease of endocrine system ()

       Child Nodes:
........expandautoimmune hepatitis ()
........expandautoimmune hypoparathyroidism (disease) ()
........expandautoimmune oophoritis ()
........expandautoimmune pancreatitis ()
........expandautoimmune polyendocrinopathy ()
........expandautoimmune primary ovarian failure ()
........expandautoimmune thyroid disease ()
........expandIgG4-related sclerosing cholangitis ()
........expandIgG4-related thyroid disease ()
........expandinsulin autoimmune syndrome ()
........expandprimary hypophysitis ()
........expandtype 1 diabetes mellitus ()



 Sister Nodes: 
..expandadrenal gland disease ()
..expandautoimmune disease of endocrine system ()
..expandcholedocholithiasis ()
..expandendocrine gland neoplasm ()
..expandendocrine tuberculosis ()
..expandestrogen resistance syndrome ()
..expandgenetic endocrine growth disease ()
..expandgonadal disease ()
..expandhyperinsulinemic hypoglycaemia ()
..expandhypoinsulinemic hypoglycemia and body hemihypertrophy ()
..expandliver disease ()
..expandmonogenic obesity ()  LSDB  L: 00114;
..expandneuroendocrine disease ()
..expandnon-neoplastic bile duct disorder ()
..expandpancreas disease ()
..expandparathyroid gland disease ()
..expandpolycystic ovary syndrome ()
..expandpolyendocrinopathy ()
..expandrare endocrine growth disease ()
..expandrare genetic hypothalamic or pituitary disease ()
..expandrare hypothalamic or pituitary disease ()
..expandrare parathyroid disease and phosphocalcic metabolism anomaly ()
..expandthymus gland disease ()
..expandthyroid gland disease ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:569
Name:autoimmune disease of endocrine system
Definition:A hypersensitivity reaction type II disease that involves the endocrine system.
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Synonyms:endocrine system autoimmune disease; endocrine system hypersensitivity reaction type II disease
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
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Phenotypes
Disease Causing ClinVar Variants
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