Erythema
Symptom Information:
Symptom ID: | HPO:0010783 | |||||||||||||||||||||||||||||||||||||||||||
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) 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) |
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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) |