raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:1057

OBSOLETE: Intracranial aneurysms-multiple congenital anomalies syndrome

inactive · referred to ORPHA:285014Rare disease with thoracic aortic aneurysm and aortic dissection

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Rare disease with thoracic aortic aneurysm and aortic dissection

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Intracranial aneurysms-multiple congenital anomalies syndrome
frOBSOLETE : Syndrome d'anévrismes crâniens-anomalies multiples
deOBSOLET: Intrakranielle Aneurysmen-multiple kongenitale Anomalien-Syndrom
esOBSOLETO: Síndrome de aneurisma intracraneal-anomalías congénitas múltiples
itOBSOLETO: Aneurismi del cranio - anomalie multiple
nlOBSOLEET: Intracraniële aneurysma's - meervoudige congenitale anomalieën-syndroom
ptOBSOLETO: Síndrome de aneurismas intracranianos-anomalias congénitas múltiplas
plNIEAKTUALNE: Tetniak wewnatrzczaszkowy - wielorakie wady wrodzone
csNEAKTUÁLNÍ: Syndrom zahrnující intrakraniální aneuryzmata a vícečetné vrozené vady
ukЗАСТАРІЛО: Синдром внутрішньочерепної аневризми - множинних вроджених аномалій
zh废弃:颅内动脉瘤-多发性先天性异常综合征
trEski adı: İntrakraniyal anevrizmalar-çoklu doğumsal anomaliler 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