ORPHA:325638
Syndrome with difference of sex development of gynecological interest
Synonyms: Syndrome with DSD of gynecological interest · Syndrome with disorder of sex development of gynecological interest
- 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 | Syndrome with difference of sex development of gynecological interest | Syndrome with DSD of gynecological interest · Syndrome with disorder of sex development of gynecological interest |
| fr | Syndrome avec différence du développement sexuel d'intérêt gynécologique | Syndrome avec ADS d'intérêt gynécologique · Syndrome avec DSD d'intérêt gynécologique · Syndrome avec anomalie du développement sexuel d'intérêt gynécologique |
| de | Syndrome mit Störung der Geschlechtsentwicklung des gynäkologischen Formenkreises | Syndrome mit DSD des gynäkologischen Fachbereichs |
| es | Síndrome con desarrollo sexual diferente de interés ginecológico | Síndrome con DSD de interés ginecológico · Síndrome con trastorno del desarrollo sexual de interés ginecológico |
| it | Sindrome associata a disturbo dello sviluppo sessuale di interesse ginecologico | Sindrome associata a DSD di interesse ginecologico |
| nl | Syndroom met geslachtsontwikkelingsstoornis van gynaecologisch belang | Syndroom met DSD van gynaecologisch belang |
| pt | Síndrome com doença do desenvolvimento sexual de interesse ginecológico | |
| pl | Zespół z zaburzeniem różnicowania płci w aspekcie ginekologicznym | Zespół z ZRP w aspekcie ginekologicznym |
| cs | Syndrom s poruchou pohlavního vývoje gynekologického typu | Syndrom s DSD gynekologického typu |
| uk | Синдром з порушенням статевої диференціації, що представляє гінекологічний інтерес | Синдром з порушенням статевого розвитку, що має гінекологічний інтерес · Синдром з ПСР, що представляє гінекологічний інтерес |
| zh | 妇科相关性发育障碍综合征 | 妇科相关DSD综合征 |
| tr | Jinekolojinin ilgillendiği 46,XY cinsiyet gelişim bozukluğu ile seyreden sendrom | Jinekoloji ile ilgili DSD ile seyreden sendrom |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17978 | E | validated | |
| UMLS | C5679864 | 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 (2):
- ORPHA:325620Difference of sex development of gynecological interest
rare gynecological and obstetric diseases - ORPHA:325665Genetic difference of sex development of gynecological interest
rare genetic diseases
Children (20):
- ORPHA:297546,XX difference of sex development-skeletal anomalies syndrome
- ORPHA:16856346,XY gonadal dysgenesis-motor and sensory neuropathy syndrome
- ORPHA:140Campomelic dysplasia
- ORPHA:1422Chondrodysplasia-difference of sex development syndrome
- ORPHA:220Denys-Drash syndrome
- ORPHA:2983Difference of sex development-intellectual disability syndrome
- ORPHA:1642Distal deletion 9p syndrome
- ORPHA:2282Dysmorphism-short stature-deafness-difference of sex development syndrome
- ORPHA:347Frasier syndrome
- ORPHA:137631Lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome
- ORPHA:3097Meacham syndrome
- ORPHA:247768Müllerian aplasia and hyperandrogenism
- ORPHA:991PAGOD syndrome
- ORPHA:85112Palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome
- ORPHA:2855Perrault syndrome
- ORPHA:199310Tetragametic chimerism syndrome
- ORPHA:881Turner syndrome
- ORPHA:893WAGR syndrome
- ORPHA:847X-linked alpha-thalassemia-intellectual disability syndrome
- ORPHA:1770XY type gonadal dysgenesis-associated anomalies syndrome
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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/325638
- This record as JSON: /data/d/325638.json