ORPHA:139024
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 | Overgrowth/obesity syndrome | |
| fr | Syndrome avec obésité/croissance excessive | |
| de | Großwuchs/Adipositas-Syndrom | |
| es | Síndrome de hipercrecimiento/obesidad | |
| it | Sindrome da iperaccrescimento/obesità | |
| nl | Overgroei-/obesitassyndroom | |
| pt | Síndrome de sobrecrescimento/obesidade | |
| pl | Zespół nadmiernego wzrostu/otyłości | |
| cs | Syndromy s makrosomií/obezitou | |
| uk | Синдром надмірного росту/ожиріння | |
| zh | 过度生长/肥胖综合征 | |
| tr | Aşırı büyüme / obezite sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15330 | E | validated | |
| UMLS | C5680619 | E | validated | |
| GARD | 19903 | 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
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/139024
- This record as JSON: /data/d/139024.json