ORPHA:281082
Inherited non-syndromic ichthyosis
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Inherited non-syndromic ichthyosis | |
| fr | Ichtyose héréditaire non syndromique | |
| de | Ichthyose, hereditäre, nicht-syndromale Form | |
| es | Ictiosis hereditaria no sindrómica | |
| it | Ittiosi ereditaria, forma non sindromica | |
| nl | Overgeërfde ichthyosis niet-syndromale vorm | |
| pt | Ictiose hereditária forma não-sindromática | |
| pl | Dziedziczna rybia łuska postać niesyndromiczna | |
| cs | Dědičné nesyndromické ichtyózy | |
| uk | Спадковий несиндромальний іхтіоз | |
| zh | 遗传性非综合征型鱼鳞病 | |
| tr | Kalıtsal sendromik-olmayan iktiyoz |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | EC20.0 | E | specific | validated |
| MONDO | 17262 | E | validated | |
| UMLS | C5681020 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:183435Inherited ichthyosis
rare genetic diseases; rare skin diseases
Children (8):
- ORPHA:281097Autosomal recessive congenital ichthyosis
- ORPHA:317Erythrokeratodermia variabilis
- ORPHA:281103Keratinopathic ichthyosis
- ORPHA:79395Keratoderma hereditarium mutilans with ichthyosis
- ORPHA:281201Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome
- ORPHA:817Peeling skin syndrome
- ORPHA:444138Peeling skin-leukonychia-acral punctate keratoses-cheilitis-knuckle pads syndrome
- ORPHA:461Recessive X-linked ichthyosis
4
Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | 1-9 / 100 000 | 1.13 / 100 000 | France | Value and class | Not yet validated | 24393603[PMID] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/281082
- This record as JSON: /data/d/281082.json