Acquired epidermolysis bullosa
General Information (adopted from Orphanet):
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Synonyms, Signs:
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Epidermolysis bullosa acquisita
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Number of Symptoms
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11
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OrphanetNr:
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46487
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OMIM Id:
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ICD-10:
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L12.3
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UMLs:
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MeSH:
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MedDRA:
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10056508
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Snomed:
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2772003
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Prevalence, inheritance and age of onset:
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Prevalence:
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No data available.
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Inheritance:
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Not applicable
[Orphanet]
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Age of onset:
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Adult
[Orphanet]
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Disease classification (adopted from Orphanet):
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Parent Diseases:
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Autoimmune bullous skin disease
-Rare skin disease
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1
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(HPO:0011830)
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Abnormality of oral mucosa |
Very frequent [Orphanet]
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47 / 7739
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2
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(HPO:0002027)
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Abdominal pain |
Occasional [Orphanet]
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|
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184 / 7739
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3
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(HPO:0002250)
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Abnormality of the large intestine |
Occasional [Orphanet]
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32 / 7739
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4
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(HPO:0001595)
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Abnormality of the hair |
Very frequent [Orphanet]
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89 / 7739
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5
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(HPO:0001025)
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Urticaria |
Occasional [Orphanet]
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73 / 7739
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6
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(HPO:0200037)
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Skin vesicle |
Very frequent [Orphanet]
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102 / 7739
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7
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(HPO:0001072)
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Thickened skin |
Occasional [Orphanet]
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87 / 7739
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8
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(HPO:0001597)
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Abnormality of the nail |
Frequent [Orphanet]
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115 / 7739
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9
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(HPO:0000987)
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Atypical scarring of skin |
Occasional [Orphanet]
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|
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58 / 7739
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10
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(HPO:0000989)
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Pruritus |
Occasional [Orphanet]
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|
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111 / 7739
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11
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(HPO:0030350)
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Erythematous papule |
Frequent [Orphanet]
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123 / 7739
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ClinVar (via SNiPA)
| Gene symbol |
Variation |
Clinical significance |
Reference |