Abnormal blistering of the skin
Symptom Information:
Symptom ID: | HPO:0008066 | |||||||||||||||||||||||||||||||||||||
Synonyms: |
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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) Abnormality of skin morphology(HPO:0011121) Abnormal blistering of the skin(HPO:0008066) MedDRA: Injury, poisoning and procedural complications(MedDRA:10022117) Injuries NEC(MedDRA:10022114) Skin injuries NEC(MedDRA:10027699) Abnormal blistering of the skin(HPO:0008066) |
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Database Frequency: | 20 / 7739 | |||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Acral peeling skin syndrome | (Orphanet:263534) |
Congenital erythropoietic porphyria | (Orphanet:79277) |
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome | (Orphanet:306504) |
Connective tissue disorder due to lysyl hydroxylase-3 deficiency | (Orphanet:300284) |
Cutaneous photosensitivity - lethal colitis | (Orphanet:2881) |
EPIDERMOLYSIS BULLOSA WITH DEFICIENCY OF GALACTOSYLHYDROXYLYSYL GLUCOSYLTRANSFERASE | (OMIM:131880) |
EPIDERMOLYSIS BULLOSA WITH DIAPHRAGMATIC HERNIA | (OMIM:226735) |
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) |
Epidermolytic ichthyosis | (Orphanet:312) |
Familial spontaneous pneumothorax | (Orphanet:2903) |
Generalized dominant dystrophic epidermolysis bullosa | (Orphanet:231568) |
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type | (Orphanet:79399) |
Junctional epidermolysis bullosa - pyloric atresia | (Orphanet:79403) |
Pemphigus vulgaris | (Orphanet:704) |
Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |
Transient bullous dermolysis of the newborn | (Orphanet:79411) |
Tyrosinemia type 2 | (Orphanet:28378) |