Skin vesicle

Symptom Information:

Symptom ID: HPO:0200037
Synonyms:
Skin vesicle [Orphanet:23310]
Skin bulla [Orphanet:23310]
Blister (morphologic abnormality) [Orphanet:23310]
Filtering bleb (morphologic abnormality) [Orphanet:23310]
Blistering eruption (disorder) [Orphanet:23310]
Bulla [Orphanet:23310]
Blistering eruption [Orphanet:23310]
Vesicles/bullous/exsudative lesions/bullous/cutaneous/mucosal detachment [Orphanet:23310]
Blister [Orphanet:23310]
Blister [MedDRA:10005191]
Blister of elbow, forearm, and wrist, without mention of infection [MedDRA:10005191]
Blister of face, neck, and scalp except eye, without mention of infection [MedDRA:10005191]
Blister of fingers, without mention of infection [MedDRA:10005191]
Blister of foot and toe(s), without mention of infection [MedDRA:10005191]
Blister of hand(s) except finger(s) alone, without mention of infection [MedDRA:10005191]
Blister of hip, thigh, leg, and ankle, without mention of infection [MedDRA:10005191]
Blister of other, multiple, and unspecified sites, without mention of infection [MedDRA:10005191]
Blister of shoulder and upper arm, without mention of infection [MedDRA:10005191]
Blister of trunk, without mention of infection [MedDRA:10005191]
Blistering [MedDRA:10005191]
Blisters [MedDRA:10005191]
Bullae [MedDRA:10005191]
Vesicle [MedDRA:10005191]
Vesicles [MedDRA:10005191]
Delayed blistering [MedDRA:10005191]
Yellow blistering [MedDRA:10005191]
Blistering [OMIM:Blistering]
Blistering (fingers, toes, pinnae) [OMIM:Blistering (fingers, toes, pinnae)]
Bullae [OMIM:Bullae]
Vesicles [OMIM:Vesicles]
Quality:
Cross references:
HPO:0008066 "Abnormal blistering of the skin" [Orphanet:23310]
Orphanet:23310 "Vesicles/bullous/exsudative lesions/bullous/cutaneous/mucosal detachment" [Orphanet:23310]
OMIM: "Blistering" [OMIM:Blistering]
OMIM: "Blistering (fingers, toes, pinnae)" [OMIM:Blistering (fingers, toes, pinnae)]
OMIM: "Bullae" [OMIM:Bullae]
OMIM: "Vesicles" [OMIM:Vesicles]
UMLS:C0005758 "Bulla" [Orphanet:23310]
UMLS:C0344311 "Blistering eruption" [Orphanet:23310]
Is a (Direct Parents):
MedDRA Skin injuries NEC
HPO         Localized skin lesion
Orphanet Abnormality of the skin
Orphanet Abnormal blistering of the skin
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)
Beh├žet 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)