raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:90022

OBSOLETE: Cardiomyopathy-renal anomalies syndrome

inactive · referred to ORPHA:167848Rare cardiomyopathy

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 cardiomyopathy

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Cardiomyopathy-renal anomalies syndrome
frOBSOLETE : Syndrome de cardiomyopathie-anomalies rénales
deOBSOLET: Kardiomyopathie - Nierenanomalien
esOBSOLETO: Síndrome de miocardiopatía-anomalías renales
itOBSOLETO: Cardiomiopatia - anomalie renali
nlOBSOLEET: Cardiomyopathie - renale anomalieën
ptOBSOLETO: Síndrome de miocardiopatia-anomalias renais
plNIEAKTUALNE: Kardiomiopatia - anomalie nerek
csNEAKTUÁLNÍ: Syndrom zahrnující kardiomyopatii a renální anomálie
ukЗАСТАРІЛО: Синдром кардіоміопатії з нирковими аномаліями
zh弃用:心肌病-肾畸形综合征
trEski adı: Kardiyomiyopati-böbrek anomalileri 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