raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:730866

Wisconsin syndrome

Synonyms: 3q24q25 deletion syndrome · Deletion 3q24q25 · Monosomy 3q24q25 · Del(3)(q24q25)

Type
Disease
Group
Disorder
Inheritance
Autosomal dominant
Status
active

Orphadata ships no English definition for this code.

1

Names in Orphadata languages

9 of 12 languages
LangNameSynonyms
enWisconsin syndrome3q24q25 deletion syndrome · Deletion 3q24q25 · Monosomy 3q24q25 · Del(3)(q24q25)
frSyndrome de WisconsinMonosomie 3q24q25 · Del(3)(q24q25) · Syndrome de délétion 3q24q25 · Délétion 3q24q25
deWisconsin-SyndromDel(3)(q24q25) · Deletion 3q24q25 · Monosomie 3q24q25 · 3q24q25-Deletionssyndrom
esSíndrome de WisconsinDel(3)(q24q25) · Deleción 3q24q25 · Monosomía 3q24q25 · Síndrome de deleción 3q24q25
itSindrome di WisconsinSindrome da delezione 3q24q25 · Del(3)(q24q25) · Delezione 3q24q25 · Monosomia 3q24q25
nlWisconsin-syndroom3q24q25-deletiesyndroom · Monosomie 3q24q25 · Deletie 3q24q25 · Del(3)(q24q25)
ptWisconsin syndrome
plWisconsin syndrome= en
csWisconsin syndrome= en
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (3):

No children.

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