Immunologic hypersensitivity
Symptom Information:
Symptom ID: | HPO:0100326 | |||||||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||||||||||||||||||||
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) Immunologic hypersensitivity(HPO:0100326) MedDRA: Immune system disorders(MedDRA:10021428) Allergic conditions(MedDRA:10001708) Allergic conditions NEC(MedDRA:10027654) Immunologic hypersensitivity(HPO:0100326) Atopic disorders(MedDRA:10052737) Immunologic hypersensitivity(HPO:0100326) |
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Database Frequency: | 28 / 7739 | |||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Acquired angioedema | (Orphanet:91385) |
Acquired ichthyosis | (Orphanet:454) |
Aggressive systemic mastocytosis | (Orphanet:98850) |
Alveolar echinococcosis | (Orphanet:284) |
Anisakiasis | (Orphanet:1070) |
Bardet-Biedl syndrome 13 | (OMIM:615990) |
Bardet-Biedl syndrome 19 | (OMIM:615996) |
Bardet-Biedl syndrome 2 | (OMIM:615981) |
Bardet-Biedl syndrome 7 | (OMIM:615984) |
Behçet disease | (Orphanet:117) |
Combined immunodeficiency due to DOCK8 deficiency | (Orphanet:217390) |
Cutaneous mastocytosis | (Orphanet:66646) |
Diffuse cutaneous mastocytosis | (Orphanet:79456) |
Distomatosis | (Orphanet:1685) |
Dracunculiasis | (Orphanet:231) |
Drug rash with eosinophilia and systemic symptoms | (Orphanet:139402) |
Dystrophic epidermolysis bullosa | (Orphanet:303) |
Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
Hereditary angioedema | (Orphanet:91378) |
Hydatidosis | (Orphanet:400) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
Hypotrichosis with juvenile macular degeneration | (Orphanet:1573) |
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome | (Orphanet:37042) |
Intestinal lymphangiectasia | (Orphanet:36204) |
Keratosis pilaris atrophicans | (Orphanet:498) |
Mastocytosis | (Orphanet:98292) |
Netherton syndrome | (Orphanet:634) |
Systemic mastocytosis | (Orphanet:2467) |