raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:1625

OBSOLETE: Deletion 4q

inactive · referred to ORPHA:262029Partial deletion of the long arm of chromosome 4 syndrome

Synonyms: OBSOLETE: Monosomy 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 deletion of the long arm of chromosome 4

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Deletion 4qOBSOLETE: Monosomy 4q
frOBSOLETE : Délétion 4qOBSOLETE : Monosomie 4q
deOBSOLET: Deletion 4qOBSOLET: Monosomie 4q
esOBSOLETO: Deleción 4qOBSOLETO: Monosomía 4q
itOBSOLETO: Delezione 4qOBSOLETO: Monosomia 4q
nlOBSOLEET: Deletie 4qOBSOLEET: Monosomie 4q
ptOBSOLETO: Deleção 4qOBSOLETO: Monossomia 4q
plNIEAKTUALNE: Delecja 4qNIEAKTUALNE: Monosomia 4q
csNEAKTUÁLNÍ: Delece 4q= en
ukЗАСТАРІЛО: Делеція 4qЗАСТАРІЛО: Моносомія 4q
zh弃用:4号染色体长臂缺失4号染色体长臂单体
trEski adı: Delesyon 4qMonozomi 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