Linear IgA dermatosis
General Information (adopted from Orphanet):
Synonyms, Signs: |
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Number of Symptoms | 8 |
OrphanetNr: | 46488 |
OMIM Id: |
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ICD-10: |
L10.8 |
UMLs: |
C0406650 |
MeSH: |
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MedDRA: |
10024515 |
Snomed: |
95330001 |
Prevalence, inheritance and age of onset:
Prevalence: | No data available. |
Inheritance: |
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Age of onset: |
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Disease classification (adopted from Orphanet):
Parent Diseases: |
Autoimmune bullous skin disease
-Rare skin disease |
Symptom Information:
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(HPO:0011830) | Abnormality of oral mucosa | Frequent [Orphanet] | 47 / 7739 | |||
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(HPO:0002024) | Malabsorption | Frequent [Orphanet] | 142 / 7739 | |||
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(HPO:0100838) | Recurrent cutaneous abscess formation | Occasional [Orphanet] | 15 / 7739 | |||
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(HPO:0010783) | Erythema | Very frequent [Orphanet] | 138 / 7739 | |||
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(HPO:0001025) | Urticaria | Occasional [Orphanet] | 73 / 7739 | |||
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(HPO:0200037) | Skin vesicle | Very frequent [Orphanet] | 102 / 7739 | |||
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(HPO:0000989) | Pruritus | Occasional [Orphanet] | 111 / 7739 | |||
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(HPO:0002960) | Autoimmunity | Very frequent [Orphanet] | 78 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
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