ORPHA:325093

46,XX difference of sex development induced by endogenous maternal-derived androgen

Synonyms: 46,XX DSD induced by endogenous maternal-derived androgen · 46,XX disorder of sex development induced by endogenous maternal-derived androgen

Type: Clinical group
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	46,XX difference of sex development induced by endogenous maternal-derived androgen	46,XX DSD induced by endogenous maternal-derived androgen · 46,XX disorder of sex development induced by endogenous maternal-derived androgen
fr	Différence du développement sexuel 46,XX due aux androgènes d'origine maternelle endogène	ADS 46,XX due aux androgènes d'origine maternelle endogène · Anomalie du développement sexuel 46,XX due aux androgènes d'origine maternelle endogène · DSD 46,XX due aux androgènes d'origine maternelle endogène
de	Störung der Geschlechtsentwicklung 46,XX, induziert durch endogenes Androgen maternalen Ursprungs	46,XX-DSD induziert durch endogenes Androgen maternalen Ursprungs
es	Desarrollo sexual diferente 46,XX inducido por exceso de andrógenos endógenos de origen materno	Trastorno del desarrollo sexual 46,XX inducido por exceso de andrógenos endógenos de origen materno · DSD 46,XX inducido por exceso de andrógenos endógenos de origen materno
it	Disturbo dello sviluppo sessuale 46,XX indotto da androgeni endogeni di origine materna	DSD 46,XX indotto da androgeni endogeni di origine materna
nl	46,XX-geslachtsontwikkelingsstoornis geïnduceerd door endogene androgenen van maternale oorsprong	46,XX-DSD geïnduceerd door endogene androgenen van maternale oorsprong
pt	Doença do desenvolvimento sexual 46,XX induzida por andrógenios de origem materna endógenos
pl	Zaburzenie różnicowania płci z kariotypem 46,XX indukowane endogennymi matczynymi androgenami	ZRP 46,XX indukowane endogennymi matczynymi androgenami
cs	46,XY porucha pohlavního vývoje indukovaná endogenním androgenem mateřského původu	46,XY DSD indukovaná endogenním androgenem mateřského původu
uk	46,XX порушення статевої диференціації, індуковане ендогенними материнськими андрогенами	46,XX порушення статевого розвитку, спричинене ендогенним материнським андрогеном · 46,XX ПСР, індукована ендогенним андрогеном материнського походження
zh	46，XX内源性母源性雄激素所致性发育障碍	46，XX内源性母源性雄激素致DSD
tr	Endojen maternal kaynaklı androjenin neden olduğu 46,XX cinsiyet gelişimi bozukluğu	Endojen maternal kaynaklı androjen fazlalığı ile indüklenen 46, XX DSD

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	17963	E		validated
UMLS	C5679875	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:93890Rare developmental defect during embryogenesis

Parents in the classifications (1):

ORPHA:9114446,XX difference of sex development induced by maternal-derived androgen
rare developmental anomalies during embryogenesis; rare urogenital diseases; rare endocrine diseases; rare gynecological and obstetric diseases

No children.

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/325093
This record as JSON: /data/d/325093.json