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Orphanet Rare Disease Ontology
Last uploaded:
July 3, 2024
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| Preferred Name | Pemphigus foliaceus | |
| Synonyms |
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| Definitions |
A rare superficial pemphigus disease characterized by multiple, pruritic, scaly, crusted cutaneous erosions, with flaky circumscribed patches, localized mostly on the face, scalp, trunk and extremities, often presenting an erythematous base. Mucosal involvement is rarely observed. |
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| ID |
http://www.orpha.net/ORDO/Orphanet_79481 |
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| definition |
A rare superficial pemphigus disease characterized by multiple, pruritic, scaly, crusted cutaneous erosions, with flaky circumscribed patches, localized mostly on the face, scalp, trunk and extremities, often presenting an erythematous base. Mucosal involvement is rarely observed.
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| definition_citation |
Orphanet
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| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=79481 |
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| has_age_of_onset |
All ages
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| hasDbXref |
UMLS:C0263313 ICD-11:EB40.1 MedDRA:10057069 ICD-10:L10.2
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| label |
Pemphigus foliaceus
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| notation |
ORPHA:79481
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| part_of | ||
| prefixIRI |
ORDO:Orphanet_79481
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| prefLabel |
Pemphigus foliaceus
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| present_in |
Germany AND has_point_prevalence_average_value : 1.001 AND has_point_prevalence_range : 1-9 / 100 000
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| treeView | ||
| subClassOf |
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