ORPHA:325546
Sex chromosome difference of sex development
Synonyms: Sex chromosome DSD · Sex chromosome 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Sex chromosome difference of sex development | Sex chromosome DSD · Sex chromosome disorder of sex development |
| fr | Différence du développement sexuel due à une différence des chromosomes sexuels | ADS due à une anomalie des gonosomes · Anomalie du développement sexuel due à une anomalie des chromosomes sexuels · Anomalie du développement sexuel due à une anomalie des gonosomes · DSD due à une anomalie des chromosomes sexuels · DSD due à une anomalie des gonosomes · ADS due à une anomalie des chromosomes sexuels |
| de | Störung der Geschlechtsentwicklung mit aberranten Geschlechtschromosomen | DSD mit Aberrationen der Geschlechtschromosomen |
| es | Desarrollo sexual diferente por anomalías del cromosoma sexual | DSD por anomalías del cromosoma sexual · Trastorno del desarrollo sexual por anomalías del cromosoma sexual |
| it | Disturbo dello sviluppo sessuale dei cromosomi sessuali | DSD dei cromosomi sessuali |
| nl | Geslachtschromosoom geslachtsontwikkelingsstoornis | Geslachtschromosoom DSD |
| pt | doença cromossómica sexual do desenvolvimento sexual | |
| pl | Zaburzenie różnicowania płci związane z chromosomem płci | ZRP związane z chromosomem płci |
| cs | Porucha pohlavního vývoje spojená s poruchami pohlavních chromozomů | DSD spojená s poruchami pohlavních chromozomů |
| uk | Порушення статевої диференціації через порушення статевих хромосом | Порушення статевого розвитку статевих хромосом · ПСР статевих хромосом |
| zh | 性染色体相关性发育障碍 | 性染色体相关DSD |
| tr | Cinsiyet gelişiminde cinsiyet kromozom bozukluğu | Cinsiyet kromozomu DSD |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0017975 | E | validated | |
| MONDO | 17975 | E | validated | |
| MeSH | D058533 | E | validated | |
| UMLS | C2936421 | 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:90771Difference of sex development
rare developmental anomalies during embryogenesis; rare urogenital diseases; rare endocrine diseases - ORPHA:325690Genetic difference of sex development
rare genetic diseases
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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/325546
- This record as JSON: /data/d/325546.json