raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:261841

Partial deletion of chromosome 19 syndrome

Synonyms: Partial monosomy of chromosome 19

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 19 syndromePartial monosomy of chromosome 19
frSyndrome de délétion partielle du chromosome 19Monosomie partielle du chromosome 19
deChromosom 19-Deletion, partiellePartielle Monosomie des Chromosoms 19
esSíndrome de deleción parcial del cromosoma 19Monosomía parcial del cromosoma 19
itSindrome delezione parziale del cromosoma 19Monosomia parziale del cromosoma 19
nlPartiële deletie van chromosoom 19-syndroomPartiële monosomie van chromosoom 19
ptMonossomia parcial do cromossoma 19
plZespół częściowej delecji chromosomu 19Cześciowa monosomia chromosomu 19
csParciální delece chromozomu 19Parciální monozomie chromozomu 19
ukЧасткова делеція хромосоми 19Часткова моносомія хромосоми 19
zh19号染色体部分缺失19号染色体部分单体
tr19. kromozomun kısmi delesyonu19. kromozomun kısmi monozomisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0016881Evalidated
MONDO16881Evalidated
UMLSC5679663Evalidated

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