Acquired ichthyosis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
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.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Acquired ichthyosis | |
| fr | Ichtyose acquise | |
| de | Ichthyose, erworbene | |
| es | Ictiosis adquirida | |
| it | Ittiosi acquisita | |
| nl | Verworven ichthyosis | |
| pt | Ictiose adquirida | |
| pl | Rybia łuska nabyta | |
| cs | Získaná ichtyóza | |
| uk | Набутий іхтіоз | |
| zh | 获得性鱼鳞病 | |
| tr | Edinsel iktiyoz |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | L85.0 | E | specific | validated |
| ICD-11 | ED50.0 | E | specific | validated |
| MONDO | 0018683 | E | validated | |
| MeSH | C538175 | E | validated | |
| UMLS | C0263386 | E | validated | |
| MedDRA | 10021199 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:79354Ichthyosis
rare skin diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
15 annotations · validated 2016-06-01| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0000958 | Dry skin | |
| HP:0008064 | Ichthyosis | |
| HP:0000989 | Pruritus | |
| Frequent (79-30%) | ||
| HP:0010783 | Erythema | |
| HP:0000962 | Hyperkeratosis | |
| HP:0100326 | Immunologic hypersensitivity | |
| HP:0000982 | Palmoplantar keratoderma | |
| HP:0200034 | Papule | |
| HP:0001581 | Recurrent skin infections | |
| Occasional (29-5%) | ||
| HP:0002960 | Autoimmunity | |
| HP:0002665 | Lymphoma | |
| HP:0006775 | Multiple myeloma | |
| HP:0002664 | Neoplasm | |
| HP:0000083 | Renal insufficiency | |
| HP:0100242 | Sarcoma | |
Run the differential on the 3 obligate / very frequent terms
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/454
- This record as JSON: /data/d/454.json