MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
Disease Browser
Parent Node:
expandimmune system disease (MONDO:0005046)
..Starting node
..expandprimary immunodeficiency disease ()

       Child Nodes:
........expandB cell deficiency ()
........expandimmune deficiency disease ()
........expandimmunodeficiency 28 ()
........expandimmunodeficiency 37 ()
........expandimmunodeficiency 39 ()
........expandimmunodeficiency 47 ()
........expandimmunodeficiency 49 ()
........expandimmunodeficiency with defective leukocyte and lymphocyte function and with response to histamine-1 antagonist ()
........expandimmunodeficiency with defective T-cell response to interleukin 1 ()
........expandimmunodeficiency without anhidrotic ectodermal dysplasia ()
........expandimmunodeficiency, X-linked, with deficiency of 115,000 Dalton surface glycoprotein ()
........expandphagocyte bactericidal dysfunction ()
........expandprimary immunodeficiency due to a defect in adaptive immunity ()
........expandprimary immunodeficiency due to a genetic defect in innate immunity ()



 Sister Nodes: 
..expandacquired immunodeficiency ()
..expandaggressive insulitis ()
..expandanti-HLA hyperimmunization ()
..expandbenign insulitis ()
..expandbone marrow disease ()
..expandcerebral toxoplasmosis ()
..expandchronic inflammatory demyelinating polyneuropathy ()
..expandgeotrichosis ()
..expandgraft versus host disease ()
..expandgranulomatosis with polyangiitis ()
..expandhypersensitivity reaction disease ()
..expandimmune deficiency with skin involvement ()
..expandimmune system cancer ()
..expandimmune system organ benign neoplasm ()
..expandimmunodeficiency disease ()
..expandimmunodeficiency-related disorder ()
..expandimmunoproliferative disorder ()
..expandinfantile-onset periodic fever-panniculitis-dermatosis syndrome ()
..expandinflammatory bowel disease ()
..expandleukocyte disease ()
..expandlymphoid system disease ()
..expandmultiple chemical sensitivity ()
..expandprimary immunodeficiency disease ()
..expandpsoriasis ()
..expandsimian acquired immunodeficiency syndrome ()
..expandspondyloarthropathy ()
..expandthrombocytopenic purpura ()
..expandthymus gland disease ()
..expandtwin to twin transfusion syndrome ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:3778
Name:primary immunodeficiency disease
Definition:A disorder in which the immune system is unable to mount an adequate immune response.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:antibody deficiency syndrome; antibody deficiency syndromes; deficiency syndrome, antibody; deficiency syndrome, immunologic; deficiency syndrome, immunological; deficiency syndromes, antibody; deficiency syndromes, immunologic; deficiency syndromes, immunological; hypoimmunity; immune deficiency di
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal