raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:180071

Unilateral aplasia of the Müllerian ducts

Synonyms: Unicornuate uterus

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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enUnilateral aplasia of the Müllerian ductsUnicornuate uterus
frAplasie unilatérale des canaux de MüllerUtérus unicorne
deAplasie des Müller-Ganges, unilateraleUterus unicornis
esAplasia unilateral del conducto de MüllerÚtero unicorne
itAplasia monolaterale del dotto MüllerianoUtero unicorne
nlUnilaterale aplasie van gang van MüllerEenhoornige baarmoeder · Uterus unicornis
ptAplasia unilateral do ducto mulleriano
plJednostronna aplazja przewodu MülleraMacica jednorożna
csJednostranná aplázie Müllerových vývodů= en
ukОдностороння аплазія мюллерових протокОднорога матка
zh单侧苗勒管发育不全单角子宫
trMüllerian kanallarının unilateral aplazisiUnikollis uterus
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10Q51.4Especificvalidated
MONDO0015831Evalidated
MONDO15831Evalidated

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 (1):

  • ORPHA:73217Müllerian aplasia
    rare developmental anomalies during embryogenesis; rare genetic diseases; rare urogenital diseases; rare gynecological and obstetric diseases; rare transplant-related disorders

Children (2):

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