ORPHA:281210
X-linked ichthyosis syndrome
- Type
- Clinical group
- Group
- Group of disorders
- Inheritance
- Not applicable, X-linked dominant, X-linked recessive
- 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 | X-linked ichthyosis syndrome | |
| fr | Ichtyose syndromique liée à l'X | |
| de | Ichthyose-Syndrom, X-chromosomales | |
| es | Síndrome de ictiosis ligada al cromosoma X | |
| it | Ittiosi sindromica legata all'X | |
| nl | X-gebonden ichthyosis-syndroom | |
| pt | Síndrome ictiose ligada ao X | |
| pl | Zespół rybiej łuski sprzężony z chromosomem X | |
| cs | X-vázané syndromy s ichtyózou | |
| uk | Х-зчеплений синдром іхтіозу | |
| zh | X连锁遗传鱼鳞病综合征 | |
| tr | X'e bağlı iktiyoz sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q80.1 | E | specific | validated |
| ICD-11 | LD27.2 | NTBT | specific | validated |
| MONDO | 0017269 | E | validated | |
| MONDO | 17269 | E | validated | |
| UMLS | C0079588 | E | validated | |
| MedDRA | 10048063 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:281085Inherited ichthyosis syndromic form
rare genetic diseases; rare skin diseases
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/281210
- This record as JSON: /data/d/281210.json