raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:261791

Partial deletion of chromosome 6 syndrome

Synonyms: Partial monosomy of chromosome 6

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 6 syndromePartial monosomy of chromosome 6
frSyndrome de délétion partielle du chromosome 6Monosomie partielle du chromosome 6
deChromosom 6-Deletion, partiellePartielle Monosomie des Chromosoms 6
esSíndrome de deleción parcial del cromosoma 6Monosomía parcial del cromosoma 6
itSindrome delezione parziale del cromosoma 6Monosomia parziale del cromosoma 6
nlPartiële deletie van chromosoom 6-syndroomPartiële monosomie van chromosoom 6
ptMonossomia parcial do cromossoma 6
plZespół częściowej delecji chromosomu 6Cześciowa monosomia chromosomu 6
csParciální delece chromozomu 6Parciální monozomie chromozomu 6
ukЧасткова делеція хромосоми 6Часткова моносомія хромосоми 6
zh6号染色体部分缺失6号染色体部分单体
tr6. kromozomun kısmi delesyonu6. kromozomun kısmi monozomisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0016871Evalidated
MONDO16871Evalidated
UMLSC5679654Evalidated

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