raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98156

Sex-chromosome number anomaly syndrome

Synonyms: Allosome number 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 number anomaly syndromeAllosome number anomaly
frSyndrome d'anomalie de nombre des gonosomesAnomalie de nombre des chromosomes sexuels
deAnomalie der GonosomenanzahlAnomale Anzahl der Geschlechtschromosomen
esSíndrome de anomalía en el número de gonosomasAnomalías en el número de cromosomas sexuales
itsindrome anomalia del numero dei cromosomi sessualiAnomalia del numero dei cromosomi sessuali
nlGonosomenaantalanomalie-syndroomGeslachtschromosomenaantalanomalie
ptAnomalia numérica dos gonossomas
plZespół aberracji liczbowych chromosomów płciowychNieprawidłowa liczba chromosomów płci
csNumerické aberace gonozomůNumerické aberace pohlavních chromozomů
ukАномалія кількості статевих хромосомАномалія кількості алосом
zh性染色体数量异常异染色体数量异常
trCinsiyet kromozom sayısı anomalisiAllozom sayı anomalisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5680212Evalidated

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 (3):

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