MSeqDR Mitochondrial Disease Portal


 
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Parent Node:
expandautoimmune disease (MONDO:0007179)
..Starting node
..expandautoimmune disease of exocrine system ()

       Child Nodes:
........expandautoimmune hepatitis ()
........expandbenign lymphoepithelial lesion of salivary gland ()
........expandSjogren syndrome ()



 Sister Nodes: 
..expandAIS2 ()
..expandAIS3 ()
..expandAIS4 ()
..expandanti-neutrophil antibody associated vasculitis ()
..expandantiphospholipid syndrome ()
..expandautoimmune disease of blood ()
..expandautoimmune disease of cardiovascular system ()
..expandautoimmune disease of ear, nose and throat ()
..expandautoimmune disease of endocrine system ()
..expandautoimmune disease of exocrine system ()
..expandautoimmune disease of gastrointestinal tract ()
..expandautoimmune disease of musculoskeletal system ()
..expandautoimmune disease of the nervous system ()
..expandautoimmune disease of urogenital tract ()
..expandautoimmune disease with skin involvement ()
..expandautoimmune disease, multisystem, infantile-onset ()
..expandautoimmune pulmonary alveolar proteinosis ()
..expandautoimmune thrombocytopenia ()
..expandCNS demyelinating autoimmune disease ()
..expandeuthyroid Graves orbitopathy ()
..expandJaccoud syndrome ()
..expandlupus erythematosus ()
..expandPFAPA syndrome ()
..expandphacolytic glaucoma ()
..expandrheumatoid lung disease ()
..expandsystemic autoimmune disease ()
..expandtype 1 diabetes nephropathy ()
..expandtype II hypersensitivity reaction disease ()
..expandtype III hypersensitivity disease ()
..expandtype IV hypersensitivity disease ()
..expandvitiligo-associated multiple autoimmune disease susceptibility 1 ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:586
Name:autoimmune disease of exocrine system
Definition:A hypersensitivity reaction type II disease that involves the exocrine system.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:exocrine system autoimmune disease; exocrine system hypersensitivity reaction type II disease
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes: ALS2;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal