Angioedema
Symptom Information:
Symptom ID: | HPO:0100665 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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 metabolism/homeostasis(HPO:0001939) Abnormality of fluid regulation(HPO:0011032) Edema(HPO:0000969) Angioedema(HPO:0100665) Abnormality of the integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Generalized abnormality of skin(HPO:0011354) Vascular skin abnormality(HPO:0011276) Angioedema(HPO:0100665) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Angioedema and urticaria(MedDRA:10002426) Angioedema(HPO:0100665) Respiratory, thoracic and mediastinal disorders(MedDRA:10038738) Upper respiratory tract disorders (excl infections)(MedDRA:10046304) Laryngeal spasm, oedema and obstruction(MedDRA:10023855) Angioedema(HPO:0100665) |
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Database Frequency: | 14 / 7739 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Acquired angioedema | (Orphanet:91385) |
Anisakiasis | (Orphanet:1070) |
Cutaneous mastocytosis | (Orphanet:66646) |
Drug rash with eosinophilia and systemic symptoms | (Orphanet:139402) |
Hereditary angioedema type 1 | (Orphanet:100050) |
Hereditary angioedema type 3 | (Orphanet:100054) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
Immunoglobulin A vasculitis | (Orphanet:761) |
Mastocytosis | (Orphanet:98292) |
Netherton syndrome | (Orphanet:634) |
Non-histaminic angioedema | (Orphanet:658) |
Renin-angiotensin-aldosterone system-blocker-induced angioedema | (Orphanet:100057) |
TRAPS syndrome | (Orphanet:32960) |
VIBRATORY ANGIOEDEMA | (OMIM:193050) |