raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:261811

Partial deletion of chromosome 10 syndrome

Synonyms: Partial monosomy of chromosome 10

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 10 syndromePartial monosomy of chromosome 10
frSyndrome de délétion partielle du chromosome 10Monosomie partielle du chromosome 10
deChromosom 10-Deletion, partiellePartielle Monosomie des Chromosoms 10
esSíndrome de deleción parcial del cromosoma 10Monosomía parcial del cromosoma 10
itSindrome delezione parziale del cromosoma 10Monosomia parziale del cromosoma 10
nlPartiële deletie van chromosoom 10-syndroomPartiële monosomie van chromosoom 10
ptMonossomia parcial do cromossoma 10
plZespół częściowej delecji chromosomu 10Cześciowa monosomia chromosomu 10
csParciální delece chromozomu 10Parciální monozomie chromozomu 10
ukЧасткова делеція хромосоми 10Часткова моносомія хромосоми 10
zh10号染色体部分缺失10号染色体部分单体
tr10. kromozomun kısmi delesyonu10. kromozomun kısmi monozomisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0016875Evalidated
MONDO16875Evalidated
UMLSC5679658Evalidated

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