Skin rash

Symptom Information:

Symptom ID: HPO:0000988
Synonyms:
Cutaneous eruption [HPO:0000988]
Eruption of skin (disorder) [Orphanet:23220]
Cutaneous eruption (morphologic abnormality) [Orphanet:23220]
Eruption [HPO:0000988]
Exanthema [Orphanet:23220]
Skin rash [OMIM:Skin rash]
Cutaneous rash [Orphanet:23220]
Rash [HPO:0000988]
Rash [Orphanet:23220]
Rash [MedDRA:10037844]
Dry rash face [MedDRA:10037844]
Dry rash neck [MedDRA:10037844]
Eruption [MedDRA:10037844]
Eruption facial [MedDRA:10037844]
Eruption of limbs [MedDRA:10037844]
Exanthem [MedDRA:10037844]
Exanthema [MedDRA:10037844]
Extensive rash of forearm [MedDRA:10037844]
Extensive rash of legs [MedDRA:10037844]
Facial rash [MedDRA:10037844]
Hand rash [MedDRA:10037844]
Neck rash [MedDRA:10037844]
Patchy rash [MedDRA:10037844]
Rash (nonspecific) [MedDRA:10037844]
Rash both legs [MedDRA:10037844]
Rash face [MedDRA:10037844]
Rash in the outer ear [MedDRA:10037844]
Rash NOS [MedDRA:10037844]
Rash on face [MedDRA:10037844]
Rash on legs &
arms [MedDRA:10037844]
Rash over arms [MedDRA:10037844]
Rash trunk &
limbs [MedDRA:10037844]
Skin eruption [MedDRA:10037844]
Skin rash [MedDRA:10037844]
Rash aggravated [MedDRA:10037844]
Rash mouth [MedDRA:10037844]
Periocular rash [MedDRA:10037844]
Efflorescence [MedDRA:10037844]
Exanthema facial [MedDRA:10037844]
Rash trunk [MedDRA:10037844]
Localised rash [MedDRA:10037844]
Localized rash [MedDRA:10037844]
Rash peripheral [MedDRA:10037844]
Rash recurrent [MedDRA:10037844]
Palmoplantar rash [MedDRA:10037844]
Rash (erythematous macules or papules) [OMIM:Rash (erythematous macules or papules)]
Skin rashes [OMIM:Skin rashes]
Quality:
Cross references:
Orphanet:23220 "Cutaneous rash" [Orphanet:23220]
OMIM: "Skin rash" [OMIM:Skin rash]
OMIM: "Rash (erythematous macules or papules)" [OMIM:Rash (erythematous macules or papules)]
OMIM: "Skin rashes" [OMIM:Skin rashes]
UMLS:C0015230 "Eruption" [HPO:0000988]
UMLS:C0015230 "Exanthema" [Orphanet:23220]
Is a (Direct Parents):
HPO         Inflammatory abnormality of the skin
HPO         Maculopapular exanthema
Orphanet Abnormality of the skin
MedDRA Rashes, eruptions and exanthems NEC
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)
                Abnormality of skin physiology(HPO:0011122)
                   Inflammatory abnormality of the skin(HPO:0011123)
                      Skin rash(HPO:0000988)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Epidermal and dermal conditions(MedDRA:10014982)
       Rashes, eruptions and exanthems NEC(MedDRA:10052566)
          Skin rash(HPO:0000988)
Database Frequency: 98 / 7739
Resource:

All diseases associated with this symptom:

Absence of fingerprints - congenital milia (Orphanet:1658)
Adult Still's disease (Orphanet:829)
Antisynthetase syndrome (Orphanet:81)
Autoimmune hemolytic anemia, warm type (Orphanet:90033)
Autosomal agammaglobulinemia (Orphanet:33110)
Autosomal dominant beta2-microglobulinic amyloidosis (Orphanet:314652)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Biotinidase deficiency (Orphanet:79241)
Blau syndrome (Orphanet:90340)
Blue rubber bleb nevus (Orphanet:1059)
CHILD syndrome (Orphanet:139)
CREST syndrome (Orphanet:90290)
Castleman disease (Orphanet:160)
Chronic mucocutaneous candidiasis (Orphanet:1334)
Chronic recurrent multifocal osteomyelitis (Orphanet:324964)
Classical mycosis fungoides (Orphanet:2584)
Cogan syndrome (Orphanet:1467)
Congenital brain dysgenesis due to glutamine synthetase deficiency (Orphanet:71278)
Congenital rubella syndrome (Orphanet:290)
Crimean-Congo hemorrhagic fever (Orphanet:99827)
Cutaneous leukocytoclastic angiitis (Orphanet:889)
Cutaneous lupus erythematosus (Orphanet:535)
DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE (OMIM:124950)
Dengue fever (Orphanet:99828)
Dracunculiasis (Orphanet:231)
Drug rash with eosinophilia and systemic symptoms (Orphanet:139402)
Ebola hemorrhagic fever (Orphanet:319218)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Epidermolysis bullosa simplex with circinate migratory erythema (Orphanet:158681)
Erdheim-Chester disease (Orphanet:35687)
Erythema elevatum diutinum (Orphanet:90000)
Erythrokeratodermia variabilis (Orphanet:317)
Fabry disease (Orphanet:324)
Familial Mediterranean fever (Orphanet:342)
Gamma heavy-chain disease (Orphanet:100026)
Gastrointestinal stromal tumor (Orphanet:44890)
Granulomatosis with polyangiitis (Orphanet:900)
HYPERZINCEMIA WITH FUNCTIONAL ZINC DEPLETION (OMIM:601979)
Hairy cell leukemia variant (Orphanet:300878)
Hartnup syndrome (Orphanet:2116)
Hodgkin lymphoma, classical (Orphanet:391)
Holocarboxylase synthetase deficiency (Orphanet:79242)
Hyperimmunoglobulinemia D with periodic fever (Orphanet:343)
Hypermethioninemia encephalopathy due to adenosine kinase deficiency (Orphanet:289290)
Hypocomplementemic urticarial vasculitis (Orphanet:36412)
Idiopathic pulmonary fibrosis (Orphanet:2032)
Immunoglobulin A vasculitis (Orphanet:761)
Incontinentia pigmenti (Orphanet:464)
Isolated agammaglobulinemia (Orphanet:229717)
Juvenile dermatomyositis (Orphanet:93672)
Juvenile idiopathic arthritis (Orphanet:92)
Kawasaki disease (Orphanet:2331)
Lassa fever (Orphanet:99824)
Lujo hemorrhagic fever (Orphanet:319213)
Lyme disease (Orphanet:91546)
Majeed syndrome (Orphanet:77297)
Malakoplakia (Orphanet:556)
Marburg hemorrhagic fever (Orphanet:99826)
Methylmalonic acidemia with homocystinuria (Orphanet:26)
Methylmalonic acidemia with homocystinuria, type cblF (Orphanet:79284)
Mevalonic aciduria (Orphanet:29)
Microscopic polyangiitis (Orphanet:727)
Mixed connective tissue disease (Orphanet:809)
Mixed-type autoimmune hemolytic anemia (Orphanet:90036)
Mucopolysaccharidosis type 2 (Orphanet:580)
Multiple carboxylase deficiency (Orphanet:148)
Multiple endocrine neoplasia type 2 (Orphanet:653)
Nakajo-Nishimura syndrome (Orphanet:2615)
Netherton syndrome (Orphanet:634)
Non-histaminic angioedema (Orphanet:658)
Non-specific interstitial pneumonia (Orphanet:91364)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
Pancreatic insufficiency - anemia - hyperostosis (Orphanet:199337)
Pediatric systemic lupus erythematosus (Orphanet:93552)
Pellagra-like skin rash-neurological manifestations (Orphanet:2837)
Polyarteritis nodosa (Orphanet:767)
Porphyria cutanea tarda (Orphanet:101330)
Porphyria due to ALA dehydratase deficiency (Orphanet:100924)
Primary cutaneous lymphoma (Orphanet:542)
Primary hyperoxaluria type 1 (Orphanet:93598)
Pseudoxanthoma elasticum (Orphanet:758)
Pyoderma gangrenosum (Orphanet:48104)
Reticular dysgenesis (Orphanet:33355)
Reynolds syndrome (Orphanet:779)
SAPHO syndrome (Orphanet:793)
Scrub typhus (Orphanet:83317)
Severe combined immunodeficiency (Orphanet:183660)
Spontaneous periodic hypothermia (Orphanet:29822)
Sweet syndrome (Orphanet:3243)
Systemic mastocytosis (Orphanet:2467)
Systemic-onset juvenile idiopathic arthritis (Orphanet:85414)
T-B+ severe combined immunodeficiency due to gamma chain deficiency (Orphanet:276)
TRAPS syndrome (Orphanet:32960)
Thymoma (Orphanet:99867)
Tumoral calcinosis (Orphanet:53715)
Typhoid (Orphanet:99745)
Wells syndrome (Orphanet:901)
X-linked agammaglobulinemia (Orphanet:47)