raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:262648

Partial duplication of chromosome 10 syndrome

Synonyms: Partial trisomy of chromosome 10

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 10 syndromePartial trisomy of chromosome 10
frSyndrome de duplication partielle du chromosome 10Trisomie partielle du chromosome 10
deChromosom 10-Duplikation, partiellePartielle Trisomie des Chromosoms 10
esSíndrome de duplicación parcial del cromosoma 10Trisomía parcial del cromosoma 10
itSindrome duplicazione parziale del cromosoma 10Trisomia parziale del cromosoma 10
nlPartiële duplicatie van chromosoom 10-syndroomPartiële trisomie van chromosoom 10
ptTrissomia parcial do cromossoma 10
plZespół częściowej duplikacji chromosomu 10Częściowa trisomia chromosomu 10
csParciální duplikace chromozomu 10Parciální trizomie chromozomu 10
ukЧасткова дуплікація хромосоми 10Часткова трисомія хромосоми 10
zh10号染色体部分重复10号染色体部分重复/三体
tr10. kromozomun kısmi duplikasyonu10. kromozomun kısmi trizomisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0016931Evalidated
MONDO16931Evalidated
UMLSC4518498Evalidated

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