raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:261801

Partial deletion of chromosome 8 syndrome

Synonyms: Partial monosomy of chromosome 8

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 8 syndromePartial monosomy of chromosome 8
frSyndrome de délétion partielle du chromosome 8Monosomie partielle du chromosome 8
deChromosom 8-Deletion, partiellePartielle Monosomie des Chromosoms 8
esSíndrome de deleción parcial del cromosoma 8Monosomía parcial del cromosoma 8
itSindrome delezione parziale del cromosoma 8Monosomia parziale del cromosoma 8
nlPartiële deletie van chromosoom 8-syndroomPartiële monosomie van chromosoom 8
ptMonossomia parcial do cromossoma 8
plZespół częściowej delecji chromosomu 8Cześciowa monosomia chromosomu 8
csParciální delece chromozomu 8Parciální monozomie chromozomu 8
ukЧасткова делеція хромосоми 8Часткова моносомія хромосоми 8
zh8号染色体部分缺失8号染色体部分单体
tr8. kromozomun kısmi delesyonu8. kromozomun kısmi monozomisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0016873Evalidated
MONDO16873Evalidated
UMLSC5679652Evalidated

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