Urticaria
Symptom Information:
Symptom ID: | HPO:0001025 | |||||||||||||||||||||||||||||||||||||||||
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 integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Generalized abnormality of skin(HPO:0011354) Vascular skin abnormality(HPO:0011276) Urticaria(HPO:0001025) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Angioedema and urticaria(MedDRA:10002426) Urticarias(MedDRA:10046736) Urticaria(HPO:0001025) |
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Database Frequency: | 73 / 7739 | |||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME | (OMIM:601859) |
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA | (OMIM:603909) |
Acquired angioedema | (Orphanet:91385) |
Acquired epidermolysis bullosa | (Orphanet:46487) |
Adult Still's disease | (Orphanet:829) |
Aggressive systemic mastocytosis | (Orphanet:98850) |
Anisakiasis | (Orphanet:1070) |
Ataxia - photosensitivity - short stature | (Orphanet:1184) |
Autoimmune lymphoproliferative syndrome | (Orphanet:3261) |
Bullous diffuse cutaneous mastocytosis | (Orphanet:280785) |
Bullous pemphigoid | (Orphanet:703) |
CINCA syndrome | (Orphanet:1451) |
Chronic granulomatous disease | (Orphanet:379) |
Classical homocystinuria | (Orphanet:394) |
Cogan syndrome | (Orphanet:1467) |
Congenital lethal erythroderma | (Orphanet:1954) |
Cutaneous leukocytoclastic angiitis | (Orphanet:889) |
Cutaneous mastocytoma | (Orphanet:79455) |
Cutaneous mastocytosis | (Orphanet:66646) |
Cutis laxa | (Orphanet:209) |
DERMODISTORTIVE URTICARIA | (OMIM:125630) |
Dermatitis herpetiformis | (Orphanet:1656) |
Diffuse cutaneous mastocytosis | (Orphanet:79456) |
Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
Erythrokeratodermia - ataxia | (Orphanet:1955) |
Erythropoietic protoporphyria | (Orphanet:79278) |
Familial cold urticaria | (Orphanet:47045) |
Gastrointestinal stromal tumor | (Orphanet:44890) |
Hennekam-Beemer syndrome | (Orphanet:2135) |
Hereditary acrokeratotic poikiloderma, Weary type | (Orphanet:2907) |
Hereditary angioedema | (Orphanet:91378) |
Hydatidosis | (Orphanet:400) |
Hyperimmunoglobulinemia D with periodic fever | (Orphanet:343) |
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia | (Orphanet:1882) |
Ichthyosis follicularis - alopecia - photophobia | (Orphanet:2273) |
Immunoglobulin A vasculitis | (Orphanet:761) |
Indolent systemic mastocytosis | (Orphanet:98848) |
Inherited epidermolysis bullosa | (Orphanet:79361) |
KID syndrome | (Orphanet:477) |
Linear IgA dermatosis | (Orphanet:46488) |
Maculopapular cutaneous mastocytosis | (Orphanet:79457) |
Mastocytosis | (Orphanet:98292) |
Muckle-Wells syndrome | (Orphanet:575) |
Multifocal muscular fibrosis - obstructed vessels | (Orphanet:2033) |
Myalgia-eosinophilia syndrome associated with tryptophan | (Orphanet:2582) |
NLRP12-associated hereditary periodic fever syndrome | (Orphanet:247868) |
Nager syndrome | (Orphanet:245) |
Netherton syndrome | (Orphanet:634) |
Odonto-onycho-dermal dysplasia | (Orphanet:2721) |
PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2 | (OMIM:615399) |
PLCG2-associated antibody deficiency and immune dysregulation | (Orphanet:300359) |
Pediatric systemic lupus erythematosus | (Orphanet:93552) |
Pellagra-like skin rash-neurological manifestations | (Orphanet:2837) |
Pemphigoid gestationis | (Orphanet:63275) |
Pemphigus vulgaris | (Orphanet:704) |
Polyarteritis nodosa | (Orphanet:767) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Relapsing polychondritis | (Orphanet:728) |
SPLENOMEGALY, CYTOPENIA, AND VISION LOSS | (OMIM:614979) |
Schnitzler syndrome | (Orphanet:37748) |
Scleroderma | (Orphanet:801) |
Sjögren-Larsson syndrome | (Orphanet:816) |
Sparse hair - short stature - skin anomalies | (Orphanet:79132) |
Spastic paraplegia - facial-cutaneous lesions | (Orphanet:2819) |
Systemic mastocytosis | (Orphanet:2467) |
Thumb deformity - alopecia - pigmentation anomaly | (Orphanet:2251) |
URTICARIA, AQUAGENIC | (OMIM:191850) |
URTICARIA, FAMILIAL LOCALIZED HEAT | (OMIM:191950) |
VULVOVAGINITIS, ALLERGIC SEMINAL | (OMIM:193450) |
Waldenström macroglobulinemia | (Orphanet:33226) |
Wells syndrome | (Orphanet:901) |
Wiskott-Aldrich syndrome | (Orphanet:906) |