raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:325632

46,XY difference of sex development of gynecological interest

Synonyms: 46,XY DSD of gynecological interest · 46,XY 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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
en46,XY difference of sex development of gynecological interest46,XY DSD of gynecological interest · 46,XY disorder of sex development of gynecological interest
frDifférence du développement sexuel 46,XY d'intérêt gynécologiqueADS 46,XY d'intérêt gynécologique · Anomalie du développement sexuel 46,XY d'intérêt gynécologique · DSD 46,XY d'intérêt gynécologique
deStörung der Geschlechtsentwicklung 46,XY, des gynäkologischen Formenkreises46,XY-DSD des gynäkologischen Fachbereichs
esDesarrollo sexual diferente 46,XY de interés ginecológicoDSD 46,XY de interés ginecológico · Trastorno del desarrollo sexual 46,XY de interés ginecológico
itDisturbo dello sviluppo sessuale 46,XY di interesse ginecologicoDSD 46,XY di interesse ginecologico
nl46,XY-geslachtsontwikkelingsstoornis van gynaecologisch belang46,XY-DSD van gynaecologisch belang
ptDoença do desenvolvimento sexual 46,XY de interesse ginecológico
plZaburzenie różnicowania płci z kariotypem 46,XY w aspekcie ginekologicznymZRP 46,XY w aspekcie ginekologicznym
cs46,XY porucha pohlavního vývoje gynekologického typu46,XY DSD gynekologického typu
uk46,XY порушення статевої диференціації, що представляє гінекологічний інтерес46,XY порушення статевого розвитку гінекологічного характеру · 46,XY ПСР гінекологічного інтересу
zh46,XY妇科相关性发育疾病46,XY妇科相关DSD
trJinekolojinin ilgillendiği 46,XY cinsiyet gelişim bozukluğuJinekoloji ile ilgili 46,XY DSD
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO17977Evalidated
UMLSC5679867Evalidated

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 (2):

Children (4):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card