ORPHA:79389
Premature aging
- 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 | Premature aging | |
| fr | Vieillissement prématuré | |
| de | Alterung, vorzeitige | |
| es | Envejecimiento prematuro | |
| it | Invecchiamento precoce | |
| nl | Vroegtijdige veroudering | |
| pt | Envelhecimento prematuro | |
| pl | Przedwczesne starzenie | |
| cs | Předčasné stárnutí | |
| uk | Передчасне старіння | |
| zh | 早衰症 | |
| tr | Erken yaşlanma |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019303 | E | validated | |
| MONDO | 19303 | E | validated | |
| MeSH | D019588 | E | validated | |
| UMLS | C0231341 | E | validated | |
| MedDRA | 10063493 | 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 (2):
- ORPHA:68346Rare genetic skin disease
rare genetic diseases - ORPHA:89826Rare skin disease
rare skin diseases
Children (16):
- ORPHA:2500Acrogeria
- ORPHA:363665Acroosteolysis-keloid-like lesions-premature aging syndrome
- ORPHA:191Cockayne syndrome
- ORPHA:2962De Barsy syndrome
- ORPHA:2047Flynn-Aird syndrome
- ORPHA:697101Fontaine progeroid syndrome
- ORPHA:2108Hallermann-Streiff syndrome
- ORPHA:740Hutchinson-Gilford progeria syndrome
- ORPHA:363618LMNA-related cardiocutaneous progeria syndrome
- ORPHA:363649Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
- ORPHA:280576Nestor-Guillermo progeria syndrome
- ORPHA:438134PCNA-related progressive neurodegenerative photosensitivity syndrome
- ORPHA:2959Progeria-short stature-pigmented nevi syndrome
- ORPHA:902Werner syndrome
- ORPHA:3455Wiedemann-Rautenstrauch syndrome
- ORPHA:220295Xeroderma pigmentosum-Cockayne syndrome complex
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/79389
- This record as JSON: /data/d/79389.json