raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:262653

Partial duplication of chromosome 11 syndrome

Synonyms: Partial trisomy of chromosome 11

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

12 of 12 languages
LangNameSynonyms
enPartial duplication of chromosome 11 syndromePartial trisomy of chromosome 11
frSyndrome de duplication partielle du chromosome 11Trisomie partielle du chromosome 11
deChromosom 11-Duplikation, partiellePartielle Trisomie des Chromosoms 11
esSíndrome de duplicación parcial del cromosoma 11Trisomía parcial del cromosoma 11
itSindrome duplicazione parziale del cromosoma 11Trisomia parziale del cromosoma 11
nlPartiële duplicatie van chromosoom 11-syndroomPartiële trisomie van chromosoom 11
ptTrissomia parcial do cromossoma 11
plZespół częściowej duplikacji chromosomu 11Częściowa trisomia chromosomu 11
csParciální duplikace chromozomu 11Parciální trizomie chromozomu 11
ukЧасткова дуплікація хромосоми 11Часткова трисомія хромосоми 11
zh11号染色体部分重复11号染色体部分三体
tr11. kromozomun kısmi duplikasyonu11. kromozomun kısmi trizomisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-11LD41.AEspecificvalidated
MONDO0016932Evalidated
MONDO16932Evalidated
UMLSC4518499Evalidated

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