Autoimmunity

Symptom Information:

Symptom ID: HPO:0002960
Synonyms:
Autoimmune disease [HPO:0002960]
Autoimmune disorders [HPO:0002960]
Autoimmune reaction [Orphanet:47560]
Autoimmune disease (disorder) [Orphanet:47560]
Autoimmune state (finding) [Orphanet:47560]
Autoimmune reaction (finding) [Orphanet:47560]
Autoimmune Diseases [Orphanet:47560]
Autoimmunity [Orphanet:47560]
Autoimmune disease [OMIM:Autoimmune disease]
Autoimmune disorders [OMIM:Autoimmune disorders]
Autoimmunity [OMIM:Autoimmunity]
Autoimmunity/autoimmune reaction/autoantibodies [Orphanet:47560]
Autoimmune disorder [Orphanet:47560]
Autoimmune disorder [MedDRA:10061664]
Autoimmune deficiency syndrome [MedDRA:10061664]
Autoimmune disease, not elsewhere classified [MedDRA:10061664]
Autoimmune disorder NOS [MedDRA:10061664]
Autoimmune disease (in some patients) [OMIM:Autoimmune disease (in some patients)]
Autoimmune disorders [MedDRA:10003816]
Quality:
Cross references:
Orphanet:47560 "Autoimmunity/autoimmune reaction/autoantibodies" [Orphanet:47560]
OMIM: "Autoimmune disease" [OMIM:Autoimmune disease]
OMIM: "Autoimmune disorders" [OMIM:Autoimmune disorders]
OMIM: "Autoimmunity" [OMIM:Autoimmunity]
OMIM: "Autoimmune disease (in some patients)" [OMIM:Autoimmune disease (in some patients)]
UMLS:C0004364 "Autoimmune Diseases" [Orphanet:47560]
UMLS:C0443146 "Autoimmune reaction" [Orphanet:47560]
UMLS:C0004368 "Autoimmunity" [Orphanet:47560]
Is a (Direct Parents):
HPO         Autoimmune antibody positivity
Orphanet Abnormality of the immune system
HPO         Abnormality of immune system physiology
MedDRA Autoimmune disorders NEC
MedDRA Immune system disorders
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of immune system physiology(HPO:0010978)
             Autoimmunity(HPO:0002960)
MedDRA:
Immune system disorders(MedDRA:10021428)
    Autoimmunity(HPO:0002960)
Database Frequency: 78 / 7739
Resource:

All diseases associated with this symptom:

22q11.2 deletion syndrome (Orphanet:567)
AUTOIMMUNE DISEASE (OMIM:109100)
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET (OMIM:615952)
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III (OMIM:615559)
Acquired ichthyosis (Orphanet:454)
Adiposis dolorosa (Orphanet:36397)
Alopecia totalis (Orphanet:700)
Anti-glomerular basement membrane disease (Orphanet:375)
Antisynthetase syndrome (Orphanet:81)
Autoimmune hemolytic anemia (Orphanet:98375)
Autoimmune hemolytic anemia, cold type (Orphanet:228312)
Autoimmune hemolytic anemia, warm type (Orphanet:90033)
Autoimmune polyendocrinopathy type 1 (Orphanet:3453)
Autosomal recessive lymphoproliferative disease (Orphanet:238505)
Bullous pemphigoid (Orphanet:703)
Bullous systemic lupus erythematosus (Orphanet:46489)
C1q DEFICIENCY (OMIM:613652)
COMPLEMENT COMPONENT 2 DEFICIENCY (OMIM:217000)
COMPLEMENT COMPONENT C1r/C1s DEFICIENCY (OMIM:216950)
CREST syndrome (Orphanet:90290)
Cernunnos-XLF deficiency (Orphanet:169079)
Cogan syndrome (Orphanet:1467)
Cold agglutinin disease (Orphanet:56425)
Combined immunodeficiency T+ B+ due to partial RAG1 deficiency (Orphanet:231154)
Cronkhite-Canada syndrome (Orphanet:2930)
Dermatitis herpetiformis (Orphanet:1656)
Dermatomyositis (Orphanet:221)
Diabetes mellitus, ketosis-prone (OMIM:612227)
Diffuse cutaneous systemic sclerosis (Orphanet:220393)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Febrile infection-related epilepsy syndrome (Orphanet:163703)
Felty syndrome (Orphanet:47612)
Gamma heavy-chain disease (Orphanet:100026)
Granulomatosis with polyangiitis (Orphanet:900)
Hereditary angioedema type 1 (Orphanet:100050)
Hypocomplementemic urticarial vasculitis (Orphanet:36412)
IMMUNODEFICIENCY 22 (OMIM:615758)
IMMUNODEFICIENCY, COMMON VARIABLE, 2 (OMIM:240500)
IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY (OMIM:614700)
IMMUNOGLOBULIN A DEFICIENCY 1 (OMIM:137100)
IMMUNOGLOBULIN A DEFICIENCY 2 (OMIM:609529)
Inclusion body myositis (Orphanet:611)
Isolated agammaglobulinemia (Orphanet:229717)
Juvenile dermatomyositis (Orphanet:93672)
Juvenile idiopathic arthritis (Orphanet:92)
Juvenile rheumatoid factor-negative polyarthritis (Orphanet:85408)
Juvenile rheumatoid factor-positive polyarthritis (Orphanet:85435)
LYMPHOPROLIFERATIVE SYNDROME 1 (OMIM:613011)
Limited cutaneous systemic sclerosis (Orphanet:220402)
Linear IgA dermatosis (Orphanet:46488)
MYASTHENIA GRAVIS (OMIM:254200)
Microscopic polyangiitis (Orphanet:727)
Mixed connective tissue disease (Orphanet:809)
Mixed-type autoimmune hemolytic anemia (Orphanet:90036)
Mucous membrane pemphigoid (Orphanet:46486)
Nodular non-suppurative panniculitis (Orphanet:33577)
Oligoarticular juvenile arthritis (Orphanet:85410)
Omenn syndrome (Orphanet:39041)
PLCG2-associated antibody deficiency and immune dysregulation (Orphanet:300359)
Partial acquired lipodystrophy (Orphanet:79087)
Pemphigus vulgaris (Orphanet:704)
Polyarteritis nodosa (Orphanet:767)
Polymyositis (Orphanet:732)
Relapsing polychondritis (Orphanet:728)
SJOGREN SYNDROME (OMIM:270150)
Scleroderma (Orphanet:801)
Secondary intestinal lymphangiectasia (Orphanet:90363)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
Sneddon syndrome (Orphanet:820)
Stiff person syndrome (Orphanet:3198)
Subcorneal pustular dermatosis (Orphanet:48377)
Syndromic multisystem autoimmune disease due to Itch deficiency (Orphanet:228426)
Systemic-onset juvenile idiopathic arthritis (Orphanet:85414)
T-CELL RECEPTOR-ALPHA/BETA DEFICIENCY (OMIM:615387)
TN POLYAGGLUTINATION SYNDROME (OMIM:300622)
Thymic tumor (Orphanet:100100)
Wiskott-Aldrich syndrome (Orphanet:906)
X-linked agammaglobulinemia (Orphanet:47)