raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:261786

Partial deletion of chromosome 5 syndrome

Synonyms: Partial monosomy of chromosome 5

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 5 syndromePartial monosomy of chromosome 5
frSyndrome de délétion partielle du chromosome 5Monosomie partielle du chromosome 5
deChromosom 5-Deletion, partiellePartielle Monosomie des Chromosoms 5
esSíndrome de deleción parcial del cromosoma 5Monosomía parcial del cromosoma 5
itSindrome delezione parziale del cromosoma 5Monosomia parziale del cromosoma 5
nlPartiële deletie van chromosoom 5-syndroomPartiële monosomie van chromosoom 5
ptMonossomia parcial do cromossoma 5
plZespół częściowej delecji chromosomu 5Cześciowa monosomia chromosomu 5
csParciální delece chromozomu 5Parciální monozomie chromozomu 5
ukЧасткова делеція хромосоми 5Часткова моносомія хромосоми 5
zh5号染色体部分缺失5号染色体部分单体
tr5. kromozomun kısmi delesyonu5. kromozomun kısmi monozomisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0016870Evalidated
MONDO16870Evalidated
UMLSC5679649Evalidated

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