ORPHA:183573
Genetic overgrowth/obesity 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 | Genetic overgrowth/obesity syndrome | |
| fr | Syndrome de croissance excessive ou d'obésité d'origine génétique | |
| de | Großwuchs/Adipositas-Syndrom, genetisch bedingtes | |
| es | Síndrome de sobrecrecimiento/obesidad de origen genético | |
| it | Sindrome genetica da iperaccrescimento/obesità | |
| nl | Genetisch overgroei-/obesitassyndroom | |
| pt | Síndrome de sobrecrescimento/obesidade genética | |
| pl | Genetyczny zespół nadmiernego wzrostu/otyłości | |
| cs | Geneticky podmíněné syndromy s makrosomií/obezitou | |
| uk | Генетично обумовлений синдром надмірного росту/ожиріння | |
| zh | 遗传性过度生长/肥胖综合征 | |
| tr | Genetik aşırı büyüme / obezite sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680552 | 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:183530Rare genetic developmental defect 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/183573
- This record as JSON: /data/d/183573.json