raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98157

Sex-chromosome structural anomaly syndrome

Synonyms: Allosome structural anomaly

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
enSex-chromosome structural anomaly syndromeAllosome structural anomaly
frSyndrome d'anomalie de structure des gonosomesAnomalie de structure des chromosomes sexuels
deAnomalie der GonosomenstukturAnomale Struktur der Geschlechtschromosomen
esSíndrome de anomalía estructural de los gonosomasAnomalías estructurales de los cromosomas sexuales
itsindrome anomalia della struttura dei gonosomiAnomalia della struttura dei cromosomi sessuali
nlGonosomen structurele anomalie-syndroomGeslachtschromosomen structurele anomalie
ptAnomalia estrutural dos gonossomas
plZespół aberracji strukturalnych chromosomów płciowychAberracje strukturalna chromosomów
csStrukturní aberace gonozomůStrukturní aberace pohlavních chromozomů
ukСтруктурна аномалія статевих хромосомСтруктурна аномалія алосом
zh性染色体结构异常异染色体结构异常
trCinsiyet kromozomu yapısal anomalisiAllozom yapısal anomalisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5680213Evalidated

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