Erythema

Symptom Information:

Symptom ID: HPO:0010783
Synonyms:
Erythematous condition (disorder) [Orphanet:23260]
Erythema (morphologic abnormality) [Orphanet:23260]
Erythema of skin (finding) [Orphanet:23260]
Erythema (finding) [Orphanet:23260]
Erythema [Orphanet:23260]
Erythema [OMIM:Erythema]
Erythema/erythematous lesions/erythroderma/polymorphous erythema [Orphanet:23260]
Erythema [MedDRA:10015150]
Erythema auricular [MedDRA:10015150]
Erythema circumocular-blepharal [MedDRA:10015150]
Erythema diffuse [MedDRA:10015150]
Erythema facial [MedDRA:10015150]
Erythema NOS [MedDRA:10015150]
Erythema oedematous [MedDRA:10015150]
Erythematous conditions [MedDRA:10015150]
Face red [MedDRA:10015150]
Localized erythema [MedDRA:10015150]
Lower legs erythematous [MedDRA:10015150]
Other specified erythematous condition [MedDRA:10015150]
Other specified erythematous conditions [MedDRA:10015150]
Red face [MedDRA:10015150]
Red neck [MedDRA:10015150]
Redness [MedDRA:10015150]
Redness facial [MedDRA:10015150]
Redness of external ear [MedDRA:10015150]
Redness of face [MedDRA:10015150]
Redness of legs [MedDRA:10015150]
Skin erythema [MedDRA:10015150]
Skin hyperaemia [MedDRA:10015150]
Skin hyperemia [MedDRA:10015150]
Skin red [MedDRA:10015150]
Unspecified erythematous condition [MedDRA:10015150]
Erythema periorbital [MedDRA:10015150]
Redness in breast [MedDRA:10015150]
Erythema ear [MedDRA:10015150]
Erythema edematous [MedDRA:10015150]
Infiltrative erythema [MedDRA:10015150]
Localised erythema [MedDRA:10015150]
Periungual erythema [MedDRA:10015150]
Erythema multiforme [MedDRA:10015218]
Erythema Multiforme [Orphanet:23260]
Erythema multiforme (disorder) [Orphanet:23260]
Erythemas [MedDRA:10015151]
Quality:
Cross references:
HPO:0001019 "Erythroderma" [Orphanet:23260]
Orphanet:23260 "Erythema/erythematous lesions/erythroderma/polymorphous erythema" [Orphanet:23260]
OMIM: "Erythema" [OMIM:Erythema]
UMLS:C0041834 "Erythema" [HPO:0010783]
UMLS:C0041834 "Erythema" [Orphanet:23260]
UMLS:C0014742 "Erythema Multiforme" [Orphanet:23260]
Is a (Direct Parents):
Orphanet Skin rash
MedDRA Erythroderma
Orphanet Erythroderma
HPO         Vascular skin abnormality
MedDRA Epidermal and dermal conditions
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)
                   Erythema(HPO:0010783)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Epidermal and dermal conditions(MedDRA:10014982)
       Erythema(HPO:0010783)
       Exfoliative conditions(MedDRA:10015664)
          Erythroderma(HPO:0001019)
             Erythema(HPO:0010783)
       Erythroderma(HPO:0001019)
             Erythema(HPO:0010783)
Database Frequency: 138 / 7739
Resource:

All diseases associated with this symptom:

ANNULAR ERYTHEMA (OMIM:106500)
Acquired ichthyosis (Orphanet:454)
Acral peeling skin syndrome (Orphanet:263534)
Acrodermatitis enteropathica, zinc deficiency type (Orphanet:37)
Aggressive systemic mastocytosis (Orphanet:98850)
Angioma serpiginosum (Orphanet:95429)
Annular epidermolytic ichthyosis (Orphanet:281139)
Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation (Orphanet:324530)
Behçet disease (Orphanet:117)
Biotinidase deficiency (Orphanet:79241)
Blau syndrome (Orphanet:90340)
Bloom syndrome (Orphanet:125)
Bullous diffuse cutaneous mastocytosis (Orphanet:280785)
Bullous impetigo (Orphanet:36237)
Bullous lichen planus (Orphanet:33408)
Bullous pemphigoid (Orphanet:703)
CHILD syndrome (Orphanet:139)
CREST syndrome (Orphanet:90290)
Chronic mucocutaneous candidiasis (Orphanet:1334)
Classical mycosis fungoides (Orphanet:2584)
Cockayne syndrome (Orphanet:191)
Cogan syndrome (Orphanet:1467)
Congenital ichthyosis - intellectual deficit - spastic quadriplegia (Orphanet:352333)
Congenital lethal erythroderma (Orphanet:1954)
Congenital non-bullous ichthyosiform erythroderma (Orphanet:79394)
Cutaneous leukocytoclastic angiitis (Orphanet:889)
Cutaneous lupus erythematosus (Orphanet:535)
Cutaneous mastocytosis (Orphanet:66646)
Cutaneous photosensitivity - lethal colitis (Orphanet:2881)
Cutis laxa (Orphanet:209)
Dermatitis herpetiformis (Orphanet:1656)
Dermatofibrosarcoma protuberans (Orphanet:31112)
Dermatomyositis (Orphanet:221)
Diffuse cutaneous mastocytosis (Orphanet:79456)
Drug rash with eosinophilia and systemic symptoms (Orphanet:139402)
ERYTHEMA NODOSUM, FAMILIAL (OMIM:132990)
ERYTHEMA OF ACRAL REGIONS (OMIM:227000)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Epidermodysplasia verruciformis (Orphanet:302)
Epidermolysis bullosa simplex due to plakophilin deficiency (Orphanet:158668)
Epidermolysis bullosa simplex with circinate migratory erythema (Orphanet:158681)
Epidermolytic ichthyosis (Orphanet:312)
Epidermolytic palmoplantar keratoderma (Orphanet:2199)
Erosive pustular dermatosis of the scalp (Orphanet:222)
Erythema elevatum diutinum (Orphanet:90000)
Erythema palmaris hereditarium (Orphanet:231031)
Erythrokeratodermia variabilis (Orphanet:317)
Erythromelalgia (Orphanet:1956)
Erythropoietic protoporphyria (Orphanet:79278)
Fabry disease (Orphanet:324)
Familial Mediterranean fever (Orphanet:342)
Familial benign chronic pemphigus (Orphanet:2841)
Focal dermal hypoplasia (Orphanet:2092)
Fountain syndrome (Orphanet:3219)
Generalized peeling skin syndrome (Orphanet:263543)
Generalized pustular psoriasis (Orphanet:247353)
Granulomatous slack skin (Orphanet:33111)
Griscelli disease type 2 (Orphanet:79477)
HYPOTRICHOSIS 6 (OMIM:607903)
Haim-Munk syndrome (Orphanet:2342)
Harlequin ichthyosis (Orphanet:457)
Hennekam-Beemer syndrome (Orphanet:2135)
Hereditary acrokeratotic poikiloderma, Weary type (Orphanet:2907)
Hereditary angioedema type 1 (Orphanet:100050)
Hereditary palmoplantar keratoderma, Gamborg-Nielsen type (Orphanet:86923)
Hydatidosis (Orphanet:400)
Hyperimmunoglobulinemia D with periodic fever (Orphanet:343)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Immunoglobulin A vasculitis (Orphanet:761)
Incontinentia pigmenti (Orphanet:464)
Jessner's lymphocytic infiltration of the skin (Orphanet:33314)
Juvenile dermatomyositis (Orphanet:93672)
KID syndrome (Orphanet:477)
Kawasaki disease (Orphanet:2331)
Keratolytic winter erythema (Orphanet:50943)
Keratosis follicularis spinulosa decalvans (Orphanet:2340)
Keratosis palmaris et plantaris - clinodactyly (Orphanet:86919)
Kindler syndrome (Orphanet:2908)
LIG4 syndrome (Orphanet:99812)
Lamellar ichthyosis (Orphanet:313)
Lichen planopilaris (Orphanet:525)
Linear IgA dermatosis (Orphanet:46488)
Lipedema (Orphanet:77243)
Lyell syndrome (Orphanet:537)
Lyme disease (Orphanet:91546)
MEDNIK syndrome (Orphanet:171851)
MELAS (Orphanet:550)
Maculopapular cutaneous mastocytosis (Orphanet:79457)
Majeed syndrome (Orphanet:77297)
Mal de Meleda (Orphanet:87503)
Microphthalmia with linear skin defects syndrome (Orphanet:2556)
Microscopic polyangiitis (Orphanet:727)
Mutilating palmoplantar keratoderma with periorificial keratotic plaques (Orphanet:659)
Nakajo-Nishimura syndrome (Orphanet:2615)
Neonatal inflammatory skin and bowel disease (Orphanet:294023)
Netherton syndrome (Orphanet:634)
Neutral lipid storage disease (Orphanet:165)
Nodular non-suppurative panniculitis (Orphanet:33577)
Non-epidermolytic palmoplantar keratoderma (Orphanet:2337)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
Omenn syndrome (Orphanet:39041)
PROTOPORPHYRIA, ERYTHROPOIETIC (OMIM:177000)
Papillon-Lefèvre syndrome (Orphanet:678)
Pemphigoid gestationis (Orphanet:63275)
Pemphigus erythematosus (Orphanet:79480)
Pityriasis rubra pilaris (Orphanet:2897)
Polycythemia vera (Orphanet:729)
Porphyria cutanea tarda (Orphanet:101330)
Primary cutaneous lymphoma (Orphanet:542)
Primary intestinal lymphangiectasia (Orphanet:90362)
Progressive symmetric erythrokeratodermia (Orphanet:316)
Pyoderma gangrenosum (Orphanet:48104)
Quinquaud's folliculitis decalvans (Orphanet:346)
Relapsing polychondritis (Orphanet:728)
Rheumatic fever (Orphanet:3099)
Rombo syndrome (Orphanet:3110)
Rothmund-Thomson syndrome (Orphanet:2909)
Rothmund-Thomson syndrome type 1 (Orphanet:221008)
STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET (OMIM:615934)
Secondary polycythemia (Orphanet:98428)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
Sjögren-Larsson syndrome (Orphanet:816)
Stern-Lubinsky-Durrie syndrome (Orphanet:3194)
Stevens-Johnson syndrome (Orphanet:36426)
Subcorneal pustular dermatosis (Orphanet:48377)
Superficial epidermolytic ichthyosis (Orphanet:455)
Sweet syndrome (Orphanet:3243)
Systemic sclerosis (Orphanet:90291)
Sézary syndrome (Orphanet:3162)
TRAPS syndrome (Orphanet:32960)
Transgrediens et progrediens palmoplantar keratoderma (Orphanet:495)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
Tumoral calcinosis (Orphanet:53715)
VIBRATORY ANGIOEDEMA (OMIM:193050)
Wells syndrome (Orphanet:901)
X-linked dominant chondrodysplasia punctata (Orphanet:35173)
Xeroderma pigmentosum (Orphanet:910)
Zunich-Kaye syndrome (Orphanet:3474)