ORPHA:222628
Hereditary poikiloderma
- 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Hereditary poikiloderma | |
| fr | Poïkilodermie héréditaire | |
| de | Poikilodermie, hereditäre | |
| es | Poiquilodermia hereditaria | |
| it | Poichilodermia ereditaria | |
| nl | Erfelijke poikilodermie | |
| pt | Poiquilodermia hereditária | |
| pl | Poikilodermia dziedziczna | |
| cs | Hereditární poikilodermie | |
| uk | Спадкова пойкилодермія | |
| zh | 遗传性皮肤异色病 | |
| tr | Kalıtsal poikiloderma |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0016382 | E | validated | |
| MONDO | 16382 | E | validated | |
| UMLS | C5680891 | 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 (2):
- ORPHA:79353Epidermal disease
rare skin diseases - ORPHA:183426Genetic epidermal disorder
rare genetic diseases
Children (7):
- ORPHA:1775Dyskeratosis congenita
- ORPHA:2907Hereditary acrokeratotic poikiloderma
- ORPHA:221043Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome
- ORPHA:221039Hereditary sclerosing poikiloderma, Weary type
- ORPHA:221046Poikiloderma with neutropenia
- ORPHA:2909Rothmund-Thomson syndrome
- ORPHA:902Werner syndrome
Codes that Orphanet moved or referred to this one:
- ORPHA:306539OBSOLETE: Hereditary acrokeratotic poikiloderma of Kindler-Weary referred to · inactive
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
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/222628
- This record as JSON: /data/d/222628.json