Urticaria

Symptom Information:

Symptom ID: HPO:0001025
Synonyms:
Hives [HPO:0001025]
Urticaria (morphologic abnormality) [Orphanet:23240]
Urticaria (disorder) [Orphanet:23240]
Urticaria [Orphanet:23240]
Urticaria [OMIM:Urticaria]
Urticaria [MedDRA:10046735]
Acute allergic urticaria [MedDRA:10046735]
Acute urticaria [MedDRA:10046735]
Allergic urticaria [MedDRA:10046735]
Erythema urticarial [MedDRA:10046735]
Generalised urticarial [MedDRA:10046735]
Generalised urticarial rash [MedDRA:10046735]
Histamine-like rash [MedDRA:10046735]
Hives [MedDRA:10046735]
Nettle rash [MedDRA:10046735]
Other specified urticaria [MedDRA:10046735]
Pharmacological urticaria [MedDRA:10046735]
Rash urticaria-like [MedDRA:10046735]
Rash urticarial [MedDRA:10046735]
Subcutaneous urticaria [MedDRA:10046735]
Unspecified urticaria [MedDRA:10046735]
Urticaria acute [MedDRA:10046735]
Urticaria aggravated [MedDRA:10046735]
Urticaria NOS [MedDRA:10046735]
Urticaria subcutaneous [MedDRA:10046735]
Urticaria, unspecified [MedDRA:10046735]
Urticarial [MedDRA:10046735]
Urticarial rash [MedDRA:10046735]
Urticarial symptom [MedDRA:10046735]
Urticated rash [MedDRA:10046735]
Urtication [MedDRA:10046735]
Welts [MedDRA:10046735]
Wheals [MedDRA:10046735]
Generalized urticaria [MedDRA:10046735]
Urticaria generalised [MedDRA:10046735]
Urticaria drug-induced [MedDRA:10046735]
Urticaria localised [MedDRA:10046735]
Urticaria localized [MedDRA:10046735]
Generalized urticarial rash [MedDRA:10046735]
Urticaria recurrent [MedDRA:10046735]
Generalised urticaria [MedDRA:10046735]
Quality:
Cross references:
Orphanet:23240 "Urticaria" [Orphanet:23240]
OMIM: "Urticaria" [OMIM:Urticaria]
UMLS:C0042109 "Urticaria" [HPO:0001025]
UMLS:C0042109 "Urticaria" [Orphanet:23240]
Is a (Direct Parents):
HPO         Vascular skin abnormality
Orphanet Skin rash
MedDRA Urticarias
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)
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)