raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:261796

Partial deletion of chromosome 7 syndrome

Synonyms: Partial monosomy of chromosome 7

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 7 syndromePartial monosomy of chromosome 7
frSyndrome de délétion partielle du chromosome 7Monosomie partielle du chromosome 7
deChromosom 7-Deletion, partiellePartielle Monosomie des Chromosoms 7
esSíndrome de deleción parcial del cromosoma 7Monosomía parcial del cromosoma 7
itSindrome delezione parziale del cromosoma 7Monosomia parziale del cromosoma 7
nlPartiële deletie van chromosoom 7-syndroomPartiële monosomie van chromosoom 7
ptMonossomia parcial do cromossoma 7
plZespół częściowej delecji chromosomu 7Cześciowa monosomia chromosomu 7
csParciální delece chromozomu 7Parciální monozomie chromozomu 7
ukЧасткова делеція хромосоми 7Часткова моносомія хромосоми 7
zh7号染色体部分缺失7号染色体部分单体
tr7. kromozomun kısmi delesyonu7. kromozomun kısmi monozomisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0016872Evalidated
MONDO16872Evalidated
UMLSC5679655Evalidated

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