ORPHA:139033
Progeroid syndrome
- 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 | Progeroid syndrome | |
| fr | Syndrome progeroïde | |
| de | Progeroid-Syndrome | |
| es | Síndrome progeroide | |
| it | Sindrome progeroide | |
| nl | Progeroïd syndroom | |
| pt | Síndrome progeróide | |
| pl | Zespół progeroidalny | |
| cs | Progeroidní syndromy | |
| uk | Прогероїдний синдром | |
| zh | 类早老综合征 | |
| tr | Progeroid sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | LD2B | E | specific | validated |
| MONDO | 0015333 | E | validated | |
| MONDO | 15333 | E | validated | |
| UMLS | C5848146 | E | validated | |
| GARD | 19906 | 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:93890Rare developmental defect during embryogenesis
rare developmental anomalies during embryogenesis
Children (26):
- ORPHA:363665Acroosteolysis-keloid-like lesions-premature aging syndrome
- ORPHA:79474Atypical Werner syndrome
- ORPHA:191Cockayne syndrome
- ORPHA:528Congenital generalized lipodystrophy
- ORPHA:508Donohue syndrome
- ORPHA:2348Familial partial lipodystrophy, Dunnigan type
- ORPHA:697101Fontaine progeroid syndrome
- ORPHA:740Hutchinson-Gilford progeria syndrome
- ORPHA:50811Lipodystrophy-intellectual disability-deafness syndrome
- ORPHA:363649Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
- ORPHA:2457Mandibuloacral dysplasia
- ORPHA:647667Mandibuloacral dysplasia associated to MTX2
- ORPHA:280576Nestor-Guillermo progeria syndrome
- ORPHA:276432Ogden syndrome
- ORPHA:438134PCNA-related progressive neurodegenerative photosensitivity syndrome
- ORPHA:2959Progeria-short stature-pigmented nevi syndrome
- ORPHA:435953Progeroid features-hepatocellular carcinoma predisposition syndrome
- ORPHA:2985Pseudoprogeria syndrome
- ORPHA:2909Rothmund-Thomson syndrome
- ORPHA:3163SHORT syndrome
- ORPHA:902Werner syndrome
- ORPHA:3455Wiedemann-Rautenstrauch syndrome
- ORPHA:659873Wormian bones-micrognathia-abnormal dentition-progeroid syndrome
- ORPHA:910Xeroderma pigmentosum
- ORPHA:90342Xeroderma pigmentosum variant
- 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/139033
- This record as JSON: /data/d/139033.json