ORPHA:90771
Difference of sex development
Synonyms: DSD · Disorder of sex development
- 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 | Difference of sex development | DSD · Disorder of sex development |
| fr | Différence du développement sexuel | ADS · Anomalie du développement sexuel · DSD |
| de | Störung der Geschlechtsentwicklung | DSD · Varianten der Geschlechtsentwicklung |
| es | Desarrollo sexual diferente | DSD · Trastorno del desarrollo sexual |
| it | Anomalie dello sviluppo sessuale | |
| nl | Geslachtsontwikkelingsstoornis | DSD |
| pt | Doença do desenvolvimento sexual | |
| pl | Zaburzenia różnicowania płci | DSD |
| cs | Porucha pohlavního vývoje | DSD |
| uk | Порушення статевої диференціації | Порушення статевого розвитку · DSD |
| zh | 性发育异常 | DSD |
| tr | Cinsiyet gelişim bozukluğu | DSD |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0002145 | E | validated | |
| MONDO | 2145 | E | validated | |
| MeSH | D012734 | E | validated | |
| UMLS | C0036875 | E | validated | |
| MedDRA | 10070597 | 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 (3):
- ORPHA:93890Rare developmental defect during embryogenesis
rare developmental anomalies during embryogenesis - ORPHA:97978Rare endocrine disease
rare endocrine diseases - ORPHA:101433Rare urogenital disease
rare urogenital 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/90771
- This record as JSON: /data/d/90771.json