raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:1651

OBSOLETE: Dennis-Cohen syndrome

inactive · referred to ORPHA:102283Multiple congenital anomalies/dysmorphic syndrome-intellectual disability

Type
Category
Group
Group of disorders
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Multiple congenital anomalies/dysmorphic syndrome-intellectual disability

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Dennis-Cohen syndrome
frOBSOLETE : Syndrome de Dennis-Cohen
deOBSOLET: Dennis-Cohen-Syndrom
esOBSOLETO: Síndrome de Dennis Cohen
itOBSOLETO: Sindrome di Dennis-Cohen
nlOBSOLEET: Syndroom van Dennis-Cohen
ptOBSOLETO: Síndrome Dennis-Cohen
plNIEAKTUALNE: Zespól Dennisa i Cohena
csNEAKTUÁLNÍ: Dennis-Cohenův syndrom
ukЗАСТАРІЛО: Синдром Денніса-Коена
zh弃用:Dennis-Cohen综合征
trEski adı: Dennis-Cohen sendromu
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

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