ORPHA:325697

Genetic 46,XX difference of sex development

Synonyms: Genetic 46,XX DSD · Genetic 46,XX 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.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Genetic 46,XX difference of sex development	Genetic 46,XX DSD · Genetic 46,XX disorder of sex development
fr	Différence du développement sexuel 46,XX d'origine génétique	ADS 46,XX d'origine génétique · Anomalie du développement sexuel 46,XX d'origine génétique · DSD 46,XX d'origine génétique
de	Störung der Geschlechtsentwicklung 46,XX, genetisch bedingte	46,XX-DSD, genetisch bedingte
es	Desarrollo sexual diferente 46,XX genético	DSD 46,XX genético · Trastorno del desarrollo sexual 46,XX genético
it	Disturbo genetico dello sviluppo sessuale 46,XX	Pseudoermafroditismo femminile genetico · DSD 46,XX genetico
nl	Genetische 46,XX-geslachtsontwikkelingsstoornis	Genetische 46,XX-DSD
pt	Doença genética 46,XX do desenvolvimento sexual
pl	Zaburzenie różnicowania płci z kariotypem 46,XX uwarunkowane genetycznie	Pseudohermafrodytyzm żeński uwarunkowany genetycznie · ZRP 46,XX uwarunkowane genetycznie
cs	Geneticky podmíněné poruchy sexuálního vývoje s karyotypem 46,XX	Geneticky podmíněný 46,XX DSD · Geneticky podmíněný ženský pseudohermafroditismus
uk	Генетичне порушення статевої диференціації 46,XX	Генетичне 46,XX порушення статевого розвитку · Генетичне 46,XX ПСР
zh	遗传性46，XX性发育障碍	遗传性46，XXDSD
tr	Genetik 46, XX cinsiyet gelişim bozukluğu	Genetik 46,XX DSD

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:93890Rare developmental defect during embryogenesis

Parents in the classifications (1):

ORPHA:325690Genetic difference of sex development
rare genetic diseases

Children (4):

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

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

Sources for this card

Orphanet page: orpha.net/en/disease/detail/325697
This record as JSON: /data/d/325697.json