raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:262201

Partial duplication of chromosome 3 syndrome

Synonyms: Partial trisomy of chromosome 3

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 3 syndromePartial trisomy of chromosome 3
frSyndrome de duplication partielle du chromosome 3Trisomie partielle du chromosome 3
deChromosom 3-Duplikation, partiellePartielle Trisomie des Chromosoms 3
esSíndrome de duplicación parcial del cromosoma 3Trisomía parcial del cromosoma 3
itSindrome duplicazione parziale del cromosoma 3Trisomia parziale del cromosoma 3
nlPartiële duplicatie van chromosoom 3-syndroomPartiële trisomie van chromosoom 3
ptTrissomia parcial do cromossoma 3
plZespół częściowej duplikacji chromosomu 3Częściowa trisomia chromosomu 3
csParciální duplikace chromozomu 3Parciální trizomie chromozomu 3
ukЧасткова дуплікація хромосоми 3Часткова трисомія за хромосомою 3
zh3号染色体部分重复3号染色体部分三体
tr3. kromozomun kısmi duplikasyonu3. kromozomun kısmi trizomisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0016923Evalidated
MONDO16923Evalidated
UMLSC4518491Evalidated

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