loading...| Preferred Name |
Acquired ichthyosis |
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| Synonyms |
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| Definitions |
A rare epidermal disease characterized by rough, dry skin with prominent, plate-like scaling. It is non-hereditary and usually arises during adulthood in the context of a variety of diseases or conditions, like various types of cancer, autoimmune diseases, endocrine disorders, nutritional deficiencies, but also as a side effect of certain medications. Severity depends on the underlying disease or condition. |
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| ID |
http://www.orpha.net/ORDO/Orphanet_454 |
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| definition |
A rare epidermal disease characterized by rough, dry skin with prominent, plate-like scaling. It is non-hereditary and usually arises during adulthood in the context of a variety of diseases or conditions, like various types of cancer, autoimmune diseases, endocrine disorders, nutritional deficiencies, but also as a side effect of certain medications. Severity depends on the underlying disease or condition. |
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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=454 |
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| has_age_of_onset |
Adult |
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| has_inheritance |
Not applicable |
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| hasDbXref |
ICD-11:ED50.0 ICD-10:L85.0 UMLS:C0263386 MeSH:C538175 |
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| label |
Acquired ichthyosis |
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| notation |
ORPHA:454 |
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| part_of | ||
| prefixIRI |
ORDO:Orphanet_454 |
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| prefLabel |
Acquired ichthyosis |
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| present_in |
Worldwide AND has_point_prevalence_range : Unknown |
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| treeView | ||
| subClassOf |