ORPHA:93461
Chromosomal disease with overgrowth
- 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 | Chromosomal disease with overgrowth | |
| fr | Anomalie chromosomique avec croissance excessive | |
| de | Chromosomale Störung mit Großwuchs | |
| es | Enfermedad cromosómica con sobrecrecimiento | |
| it | Malattia cromosomica con gigantismo | |
| nl | Chromosomale ziekte met overgroei | |
| pt | Cromossomopatia com sobrecrescimento | |
| pl | Choroba chromosomalna z nadmiernym wzrostem | |
| cs | Chromozomální onemocnění s nadměrným vzrůstem | |
| uk | Хромосомне захворювання з надмірним ростом | |
| zh | 伴染色体过度生长症 | |
| tr | Aşırı büyüme ile seyreden kromozomal hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681595 | 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:93460Overgrowth syndrome
rare developmental anomalies during embryogenesis; rare genetic 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/93461
- This record as JSON: /data/d/93461.json