raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:261826

Partial deletion of chromosome 16 syndrome

Synonyms: Partial monosomy of chromosome 16

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 16 syndromePartial monosomy of chromosome 16
frSyndrome de délétion partielle du chromosome 16Monosomie partielle du chromosome 16
deChromosom 16-Deletion, partiellePartielle Monosomie des Chromosoms 16
esSíndrome de deleción parcial del cromosoma 16Monosomía parcial del cromosoma 16
itSindrome delezione parziale del cromosoma 16Monosomia parziale del cromosoma 16
nlPartiële deletie van chromosoom 16-syndroomPartiële monosomie van chromosoom 16
ptMonossomia parcial do cromossoma 16
plZespół częściowej delecji chromosomu 16Cześciowa monosomia chromosomu 16
csParciální delece chromozomu 16Parciální monozomie chromozomu 16
ukЧасткова делеція хромосоми 16Часткова моносомія хромосоми 16
zh16号染色体部分缺失16号染色体部分单体
tr16. kromozomun kısmi delesyonu16. kromozomun kısmi monozomisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0016878Evalidated
MONDO16878Evalidated
UMLSC5679657Evalidated

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