raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:1739

OBSOLETE: Duplication 4q

inactive · referred to ORPHA:262860Partial duplication of the long arm of chromosome 4 syndrome

Synonyms: OBSOLETE: Trisomy 4q

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Partial duplication of the long arm of chromosome 4

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Duplication 4qOBSOLETE: Trisomy 4q
frOBSOLETE : Duplication 4qOBSOLETE : Trisomie 4q
deOBSOLET: Duplikation 4qOBSOLET: Trisomie 4q
esOBSOLETO: Duplicación 4qOBSOLETO: Trisomía 4q
itOBSOLETO: Duplicazione 4qOBSOLETO: Trisomia 4q
nlOBSOLEET: Duplicatie 4qOBSOLEET: Trisomie 4q
ptOBSOLETO: Duplicação 4qOBSOLETO: Trissomia 4q
plNIEAKTUALNE: Duplikacja 4qNIEAKTUALNE: Trisomia 4q
csNEAKTUÁLNÍ: Duplikace 4q= en
ukЗАСТАРІЛО: Дуплікація 4qЗАСТАРІЛО: Трисомія 4q
zh弃用:4号染色体长臂重复4号染色体长臂三体
trEski adı: Duplikasyon 4qTrizomi 4q
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

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