ORPHA:90776
46,XX difference of sex development induced by fetal androgens excess
Synonyms: 46,XX DSD induced by fetal androgens excess · 46,XX disorder of sex development induced by fetal androgens excess
- 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 | 46,XX difference of sex development induced by fetal androgens excess | 46,XX DSD induced by fetal androgens excess · 46,XX disorder of sex development induced by fetal androgens excess |
| fr | Différence du développement sexuel 46,XX due à un excès d'androgènes foetal | ADS 46,XX due à un excès d'androgènes foetal · Anomalie du développement sexuel 46,XX due à un excès d'androgènes foetal · DSD 46,XX due à un excès d'androgènes foetal |
| de | 46,XX-DSD induziert durch fetalen Androgenexzess | Störung der Geschlechtsentwicklung 46,XX, durch fetalen Androgenexzess |
| es | Desarrollo sexual diferente 46,XX inducido por exceso de andrógenos de origen fetal | DSD 46,XX inducido por exceso de andrógenos de origen fetal · Trastorno del desarrollo sexual 46,XX inducido por exceso de andrógenos de origen fetal |
| it | Disturbo dello sviluppo sessuale 46,XX da eccesso fetale di androgeni | DSD 46,XX indotto da eccesso fetale di androgeni |
| nl | 46,XX-geslachtsontwikkelingsstoornis geïnduceerd door overmaat aan foetale androgenen | 46,XX-DSD geïnduceerd door overmaat aan foetale androgenen |
| pt | Doença do desenvolvimento sexual 46,XX induzido por excesso de androgénio de origem fetal | |
| pl | Zaburzenie różnicowania płci z kariotypem 46,XX indukowane nadmiarem androgenów u płodu | 46,XX DSD indukowane nadmiarem androgenów u płodu |
| cs | 46,XX porucha pohlavního vývoje vyvolaná nadbytkem fetálních androgenů | 46,XX DSD vyvolaná nadbytkem fetálních androgenů |
| uk | 46,XX порушення статевої диференціації, спричинене надлишком фетальних андрогенів | 46,XX порушення статевого розвитку, спричинене надлишком андрогенів у плода · 46,XX ПСР, індукована надлишком фетальних андрогенів |
| zh | 胎儿雄激素过多所致女性假两性畸形 | 胎儿雄激素过多所致女性假两性畸形 |
| tr | Fetal androjen fazlalığının neden olduğu 46,XX cinsiyet gelişim bozukluğu | Fetal androjen fazlalığı ile indüklenen 46, XX DSD |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680189 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (3):
- ORPHA:9807846,XX difference of sex development induced by androgens excess
rare developmental anomalies during embryogenesis; rare urogenital diseases; rare endocrine diseases; rare gynecological and obstetric diseases - ORPHA:325697Genetic 46,XX difference of sex development
rare genetic diseases - ORPHA:325665Genetic difference of sex development of gynecological interest
rare genetic diseases
Children (6):
- ORPHA:63269Antley-Bixler syndrome with genital anomaly and disorder of steroidogenesis
- ORPHA:90794Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- ORPHA:90795Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency
- ORPHA:90791Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency
- ORPHA:95699Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency
- ORPHA:786Generalized glucocorticoid resistance syndrome
4
Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/90776
- This record as JSON: /data/d/90776.json