ORPHA:371176
Congenital disorder of glycosylation with dilated cardiomyopathy
Synonyms: CDG with dilated cardiomyopathy
- Type
- Category
- Group
- Group of disorders
- Status
- active
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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital disorder of glycosylation with dilated cardiomyopathy | CDG with dilated cardiomyopathy |
| fr | Anomalie congénitale de la glycosylation avec cardiomyopathie dilatée | CDG avec cardiomyopathie dilatée |
| de | Kongenitale Glykosylierungsstörung mit dilatativer Kardiomyopathie | CDG mit dilatativer Kardiomyopathie |
| es | Trastorno congénito de la glicosilación con miocardiopatía dilatada | CDG con miocardiopatía dilatada |
| it | Disturbo congenito della glicosilazione con cardiomiopatia dilatativa | CDG con cardiomiopatia dilatativa |
| nl | Congenitale glycosylatiestoornis met gedilateerde cardiomyopathie | CDG met gedilateerde cardiomyopathie |
| pt | Doença congénita de glicosilação com cardiomiopatia dilatada | |
| pl | Wrodzone zaburzenie glikozylacji z kardiomiopatią rozstrzeniową | CDG z kardiomiopatią rozstrzeniową |
| cs | Vrozená porucha glykosylace s dilatační kardiomyopatií | CDG s dilatační kardiomyopatií |
| uk | Вроджене порушення глікозилювання з дилатаційною кардіоміопатією | CDG з дилатаційною кардіоміопатією |
| zh | 先天性糖基化障碍伴扩张型心肌病 | CDG伴扩张型心肌病 |
| tr | Dilate kardiyomiyopati ile seyreden doğumsal glikozilasyon bozukluğu | Dilate kardiyomiyopati ile seyreden CDG |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18289 | E | validated | |
| UMLS | C5679907 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:217607Familial dilated cardiomyopathy
rare cardiac diseases; rare genetic diseases - ORPHA:506225Rare disorder potentially indicated for heart transplant
rare transplant-related disorders
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/371176
- This record as JSON: /data/d/371176.json