Skin vesicle
Symptom Information:
Symptom ID: | HPO:0200037 | ||||||||||||||||||||||||||||||
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) Localized skin lesion(HPO:0011355) Skin vesicle(HPO:0200037) MedDRA: Injury, poisoning and procedural complications(MedDRA:10022117) Injuries NEC(MedDRA:10022114) Skin injuries NEC(MedDRA:10027699) Skin vesicle(HPO:0200037) |
||||||||||||||||||||||||||||||
Database Frequency: | 102 / 7739 | ||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
Acquired epidermolysis bullosa | (Orphanet:46487) |
Acral dystrophic epidermolysis bullosa | (Orphanet:158673) |
Acrodermatitis enteropathica, zinc deficiency type | (Orphanet:37) |
Autosomal dominant hyper-IgE syndrome | (Orphanet:2314) |
Autosomal recessive epidermolysis bullosa simplex | (Orphanet:89838) |
Behçet disease | (Orphanet:117) |
Bullous diffuse cutaneous mastocytosis | (Orphanet:280785) |
Bullous dystrophy, macular type | (Orphanet:1867) |
Bullous impetigo | (Orphanet:36237) |
Bullous lichen planus | (Orphanet:33408) |
Bullous pemphigoid | (Orphanet:703) |
Bullous systemic lupus erythematosus | (Orphanet:46489) |
Castleman disease | (Orphanet:160) |
Centripetalis recessive dystrophic epidermolysis bullosa | (Orphanet:89841) |
Cockayne syndrome | (Orphanet:191) |
Congenital erythropoietic porphyria | (Orphanet:79277) |
Connective tissue disorder due to lysyl hydroxylase-3 deficiency | (Orphanet:300284) |
Cutaneous lupus erythematosus | (Orphanet:535) |
Cutaneous mastocytoma | (Orphanet:79455) |
Cutaneous mastocytosis | (Orphanet:66646) |
Cutaneous photosensitivity - lethal colitis | (Orphanet:2881) |
Cutis laxa | (Orphanet:209) |
Darier disease | (Orphanet:218) |
Dermatitis herpetiformis | (Orphanet:1656) |
Diffuse cutaneous mastocytosis | (Orphanet:79456) |
Dracunculiasis | (Orphanet:231) |
Dyskeratosis congenita | (Orphanet:1775) |
Dystrophic epidermolysis bullosa | (Orphanet:303) |
Dystrophic epidermolysis bullosa pruriginosa | (Orphanet:89843) |
Dystrophic epidermolysis bullosa, nails only | (Orphanet:158676) |
EPIDERMOLYSIS BULLOSA WITH DIAPHRAGMATIC HERNIA | (OMIM:226735) |
Epidermolysis bullosa simplex | (Orphanet:304) |
Epidermolysis bullosa simplex due to plakophilin deficiency | (Orphanet:158668) |
Epidermolysis bullosa simplex superficialis | (Orphanet:89839) |
Epidermolysis bullosa simplex with anodontia/hypodontia | (Orphanet:2325) |
Epidermolysis bullosa simplex with circinate migratory erythema | (Orphanet:158681) |
Epidermolysis bullosa simplex with mottled pigmentation | (Orphanet:79397) |
Epidermolysis bullosa simplex with muscular dystrophy | (Orphanet:257) |
Epidermolysis bullosa simplex with pyloric atresia | (Orphanet:158684) |
Epidermolysis bullosa simplex, Dowling-Meara type | (Orphanet:79396) |
Epidermolysis bullosa simplex, Ogna type | (Orphanet:79401) |
Epidermolytic ichthyosis | (Orphanet:312) |
Erythema elevatum diutinum | (Orphanet:90000) |
Erythrokeratodermia variabilis | (Orphanet:317) |
Familial benign chronic pemphigus | (Orphanet:2841) |
Familial spontaneous pneumothorax | (Orphanet:2903) |
Generalized dominant dystrophic epidermolysis bullosa | (Orphanet:231568) |
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type | (Orphanet:79399) |
Generalized junctional epidermolysis bullosa, non-Herlitz type | (Orphanet:79402) |
Hartnup syndrome | (Orphanet:2116) |
Hereditary acrokeratotic poikiloderma, Weary type | (Orphanet:2907) |
Hereditary coproporphyria | (Orphanet:79273) |
Hereditary hypotrichosis with recurrent skin vesicles | (Orphanet:217407) |
Incontinentia pigmenti | (Orphanet:464) |
Inherited epidermolysis bullosa | (Orphanet:79361) |
Intestinal lymphangiectasia | (Orphanet:36204) |
Junctional epidermolysis bullosa | (Orphanet:305) |
Junctional epidermolysis bullosa - pyloric atresia | (Orphanet:79403) |
Junctional epidermolysis bullosa inversa | (Orphanet:79405) |
Junctional epidermolysis bullosa, non-Herlitz type | (Orphanet:89840) |
Kindler syndrome | (Orphanet:2908) |
Late-onset junctional epidermolysis bullosa | (Orphanet:79406) |
Lethal acantholytic epidermolysis bullosa | (Orphanet:158687) |
Lichen planopilaris | (Orphanet:525) |
Linear IgA dermatosis | (Orphanet:46488) |
Lipoid proteinosis | (Orphanet:530) |
Localized epidermolysis bullosa simplex | (Orphanet:79400) |
Lyell syndrome | (Orphanet:537) |
Majeed syndrome | (Orphanet:77297) |
Mastocytosis | (Orphanet:98292) |
Mucous membrane pemphigoid | (Orphanet:46486) |
Multiple carboxylase deficiency | (Orphanet:148) |
Non-epidermolytic palmoplantar keratoderma | (Orphanet:2337) |
Oral erosive lichen | (Orphanet:31142) |
Pachyonychia congenita | (Orphanet:2309) |
Paraneoplastic pemphigus | (Orphanet:63455) |
Peeling skin syndrome | (Orphanet:817) |
Pemphigus erythematosus | (Orphanet:79480) |
Pemphigus vulgaris | (Orphanet:704) |
Porphyria | (Orphanet:738) |
Porphyria cutanea tarda | (Orphanet:101330) |
Porphyria due to ALA dehydratase deficiency | (Orphanet:100924) |
Porphyria variegata | (Orphanet:79473) |
Pretibial dystrophic epidermolysis bullosa | (Orphanet:79410) |
Primary cutaneous lymphoma | (Orphanet:542) |
Pseudoxanthomatous diffuse cutaneous mastocytosis | (Orphanet:280794) |
Pyoderma gangrenosum | (Orphanet:48104) |
Recessive dystrophic epidermolysis bullosa inversa | (Orphanet:79409) |
Recessive dystrophic epidermolysis bullosa-generalized other | (Orphanet:89842) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Secondary intestinal lymphangiectasia | (Orphanet:90363) |
Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |
Stevens-Johnson syndrome | (Orphanet:36426) |
Superficial epidermolytic ichthyosis | (Orphanet:455) |
Superficial pemphigus | (Orphanet:46485) |
Sweet syndrome | (Orphanet:3243) |
Syringocystadenoma papilliferum | (Orphanet:840) |
Transient bullous dermolysis of the newborn | (Orphanet:79411) |
Tyrosinemia type 2 | (Orphanet:28378) |
Wells syndrome | (Orphanet:901) |
Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome | (Orphanet:65282) |