raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:262687

Partial duplication of chromosome 19 syndrome

Synonyms: Partial trisomy of chromosome 19

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 19 syndromePartial trisomy of chromosome 19
frSyndrome de duplication partielle du chromosome 19Trisomie partielle du chromosome 19
deChromosom 19-Duplikation, partiellePartielle Trisomie des Chromosoms 19
esSíndrome de duplicación parcial del cromosoma 19Trisomía parcial del cromosoma 19
itSindrome duplicazione parziale del cromosoma 19Trisomia parziale del cromosoma 19
nlPartiële duplicatie van chromosoom 19-syndroomPartiële trisomie van chromosoom 19
ptTrissomia parcial do cromossoma 19
plZespół częściowej duplikacji chromosomu 19Częściowa trisomia chromosomu 19
csParciální duplikace chromozomu 19Parciální trizomie chromozomu 19
ukЧасткова дуплікація хромосоми 19Часткова трисомія хромосоми 19
zh19号染色体部分重复19号染色体部分三体
tr19. kromozomun kısmi duplikasyonu19. kromozomun kısmi trizomisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0016937Evalidated
MONDO16937Evalidated
UMLSC4518507Evalidated

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