raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:180106

Bicervical bicornuate uterus and blind hemivagina

Type
Clinical subtype
Group
Subtype of disorder
Status
active

Orphadata ships no English definition for this code.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enBicervical bicornuate uterus and blind hemivagina
frUtérus bicorne bicervical avec rétention menstruelle unilatéraleUtérus bicorne bicervical avec hémivagin borgne
deBizervikaler Uterus bicornis und blind endende Hemivagina
esÚtero bicorne bicervical y hemivagina ciega
itUtero bicorne bicervicale ed emivagina ciecaUtero bicorne bicervicale con ritenzione mestruale monolaterale
nlBicervicale tweehoornige baarmoeder en blinde hemivagina
ptÚtero bicórneo bicervical e hemi-vagina cega
plMacica dwurożna dwuszyjkowa z niedrożną pochwą szczątkowąMacica dwurożna dwuszyjkowa one-eyed hemi-vagina
csUterus bicornis bicollis a slepá hemivagina
ukБіцервікальна дворога матка та сліпа гемівагіна
zh双宫颈双角子宫伴盲端半阴道
trBikervikal bicornuat uterus ve kör hemivajina
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10Q51.1NTBTattributedvalidated
ICD-11LB44.3NTBTindexvalidated
MONDO0015835Evalidated
UMLSC5680489Evalidated

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:180086Didelphys uterus
    rare developmental anomalies during embryogenesis; rare urogenital diseases; rare gynecological and obstetric diseases; rare transplant-related disorders

No children.

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