raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:261776

Partial deletion of chromosome 3 syndrome

Synonyms: Partial monosomy of chromosome 3

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 3 syndromePartial monosomy of chromosome 3
frSyndrome de délétion partielle du chromosome 3Monosomie partielle du chromosome 3
deChromosom 3-Deletion, partiellePartielle Monosomie des Chromosoms 3
esSíndrome de deleción parcial del cromosoma 3Monosomía parcial del cromosoma 3
itSindrome delezione parziale del cromosoma 3Monosomia parziale del cromosoma 3
nlPartiële deletie van chromosoom 3-syndroomPartiële monosomie van chromosoom 3
ptMonossomia parcial do cromossoma 3
plZespół częściowej delecji chromosomu 3Cześciowa monosomia chromosomu 3
csParciální delece chromozomu 3Parciální monozomie chromozomu 3
ukЧасткова делеція хромосоми 3Часткова моносомія хромосоми 3
zh3号染色体部分缺失3号染色体部分单体
tr3. kromozomun kısmi delesyonu3. kromozomun kısmi monozomisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0016868Evalidated
MONDO16868Evalidated
UMLSC5679651Evalidated

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