Skin rash
Symptom Information:
Symptom ID: | HPO:0000988 | |||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
|
|||||||||||||||||||||||||||||||||||||||||||||||||
Quality: | ||||||||||||||||||||||||||||||||||||||||||||||||||
Cross references: |
|
|||||||||||||||||||||||||||||||||||||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||||||||||||||||||||||||||||||||||||
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) |