raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:96136

OBSOLETE: Non-distal monosomy 7p

inactive · referred to ORPHA:261911Partial deletion of the short arm of chromosome 7 syndrome

Synonyms: OBSOLETE: Non-distal deletion 7p · OBSOLETE: Non-telomeric monosomy 7p

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 short arm of chromosome 7

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Non-distal monosomy 7pOBSOLETE: Non-distal deletion 7p · OBSOLETE: Non-telomeric monosomy 7p
frOBSOLETE : Monosomie non distale 7pOBSOLETE : Délétion non distale 7p · OBSOLETE : Monosomie non télomérique 7p
deOBSOLET: Monosomie 7p, nicht-distaleOBSOLET: Deletion 7p, nicht-distale
esOBSOLETO: Monosomía intersticial 7pOBSOLETO: Deleción intersticial 7p · OBSOLETO: Monosomía intersticial 7p
itOBSOLETO: Monosomia 7p non distaleOBSOLETO: Delezione 7p non distale · OBSOLETO: Monosomia 7p non telomerica
nlOBSOLEET: Niet-distale monosomie 7pOBSOLEET: Niet-distale deletie 7p · OBSOLEET: Niet-telomerische monosomie 7p
ptOBSOLETO: Monossomia não-distal 7p
plNIEAKTUALNE: Monosomia interstycjalna 7pNIEAKTUALNE: Monosomia nietelomerowa 7p · NIEAKTUALNE: Delecja interstycjalna 7p
csNEAKTUÁLNÍ: Non-distální monozomie 7qNEAKTUÁLNÍ: Non-distální delece 7q · NEAKTUÁLNÍ: Non-telomerická monozomie 7q
ukЗАСТАРІЛО: Недистальна моносомія 7pЗАСТАРІЛО: Недистальна делеція 7p · ЗАСТАРІЛО: Нетеломерна моносомія 7p
zh弃用:7号染色体短臂非远端单体7号染色体短臂非端粒单体
trEski adı: Distal olmayan monozomi 7pDistal olmayan delesyon 7p · Telomerik olmayan monozomi 7p
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