Autoimmunity
Symptom Information:
Symptom ID: | HPO:0002960 | |||||||||||||||||||
Synonyms: |
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Cross references: |
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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 immune system(HPO:0002715) Abnormality of immune system physiology(HPO:0010978) Autoimmunity(HPO:0002960) MedDRA: Immune system disorders(MedDRA:10021428) Autoimmunity(HPO:0002960) |
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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) |