raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:261816

Partial deletion of chromosome 11 syndrome

Synonyms: Partial monosomy of chromosome 11

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 deletion of chromosome 11 syndromePartial monosomy of chromosome 11
frSyndrome de délétion partielle du chromosome 11Monosomie partielle du chromosome 11
deChromosom 11-Deletion, partiellePartielle Monosomie des Chromosoms 11
esSíndrome de deleción parcial del cromosoma 11Monosomía parcial del cromosoma 11
itSindrome delezione parziale del cromosoma 11Monosomia parziale del cromosoma 11
nlPartiële deletie van chromosoom 11-syndroomPartiële monosomie van chromosoom 11
ptMonossomia parcial do cromossoma 11
plZespół częściowej delecji chromosomu 11Cześciowa monosomia chromosomu 11
csParciální delece chromozomu 11Parciální monozomie chromozomu 11
ukЧасткова делеція хромосоми 11Часткова моносомія хромосоми 11
zh11号染色体部分缺失11号染色体部分单体
tr11. kromozomun kısmi delesyonu11. kromozomun kısmi monozomisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0016876Evalidated
MONDO16876Evalidated
UMLSC5679659Evalidated

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