raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98732

OBSOLETE: Syndrome associated with a congenital cardiopathy

inactive · referred to ORPHA:156532Rare syndrome with cardiac malformations

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 Rare syndrome with cardiac malformations

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Syndrome associated with a congenital cardiopathy
frOBSOLETE : Syndrome avec cardiopathie congénitale
deOBSOLET: Kardiopathie-assoziiertes Syndrom, kongenitales
esOBSOLETO: Síndrome asociado a cardiopatía congénita
itOBSOLETO: Sindrome congenita associata a cardiopatia
nlOBSOLEET: Syndroom geassocieerd met congenitale cardiopathie
ptOBSOLETO: Síndrome associado a cardiopatia, congénito
plNIEAKTUALNE: Zespól zwiazany z wrodzona kardiomiopatia
csNEAKTUÁLNÍ: Syndromy spojené s vrozenou kardiopatií
ukЗАСТАРІЛО: Синдром, повязаний з вродженою кардіопатією
zh弃用:先天性心脏病相关综合征
trEski adı: Doğumsal kardiyopati ilişkili sendrom
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