raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:617307

Rare disorder related to monochorionic twin pregnancy

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

10 of 12 languages
LangNameSynonyms
enRare disorder related to monochorionic twin pregnancy
frMaladie rare liée à la grossesse gémellaire monochoriale
deSeltene Störung im Zusammenhang mit einer monochorionischen Zwillingsschwangerschaft
esTrastorno raro relacionado con el embarazo gemelar monocorialTrastorno raro relacionado con el embarazo gemelar monocoriónico
itMalattia rara correlata alla gravidanza gemellare monocoriale
nlZeldzame aandoening gerelateerd aan monochoriale tweelingzwangerschap
ptDoença rara relacionada com gestação gemelar monocoriónica
plRzadkie zaburzenie związane z ciążą bliźniaczą jednokosmówkową
csVzácná porucha související s monochoriálním dvojčetným těhotenstvím
ukРідкісний розлад, повязаний з вагітністю монохоріальною двійнею
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5681821Evalidated

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):

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