raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:262633

Partial duplication of chromosome 7 syndrome

Synonyms: Partial trisomy of chromosome 7

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 7 syndromePartial trisomy of chromosome 7
frSyndrome de duplication partielle du chromosome 7Trisomie partielle du chromosome 7
deChromosom 7-Duplikation, partiellePartielle Trisomie des Chromosoms 7
esSíndrome de duplicación parcial del cromosoma 7Trisomía parcial del cromosoma 7
itSindrome duplicazione parziale del cromosoma 7Trisomia parziale del cromosoma 7
nlPartiële duplicatie van chromosoom 7-syndroomPartiële trisomie van chromosoom 7
ptTrissomia parcial do cromossoma 7
plZespół częściowej duplikacji chromosomu 7Częściowa trisomia chromosomu 7
csParciální duplikace chromozomu 7Parciální trizomie chromozomu 7
ukЧасткова дуплікація хромосоми 7Часткова трисомія хромосоми 7
zh7号染色体部分重复7号染色体部分三体
tr7. kromozomun kısmi duplikasyonu7. kromozomun kısmi trizomisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0016928Evalidated
MONDO16928Evalidated
UMLSC4518496Evalidated

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