ORPHA:506225
Rare disorder potentially indicated for heart transplant
- 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 | Rare disorder potentially indicated for heart transplant | |
| fr | Maladie rare possiblement indiquée pour la transplantation cardiaque | |
| de | Seltene Erkrankung zur potentiellen Herz-Transplantation indiziert | |
| es | Trastorno raro potencialmente indicado para trasplante cardíaco | |
| it | Malattia rara con indicazione al trapianto cardiaco | |
| nl | Zeldzame aandoening mogelijk geïndiceerd voor harttransplantatie | |
| pt | Doença rara com potencial indicação para transplante cardíaco | |
| pl | Choroba rzadka będąca potencjalnym wskazaniem do przeszczepu serca | |
| cs | Vzácná porucha indikovaná k transplantaci srdce | |
| uk | Рідкісне захворювання, яке може бути показанням для трансплантації серця | |
| zh | 可能适用于心脏移植的罕见疾病 | |
| tr | Potansiyel olarak kalp nakli için endike olan nadir hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681216 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
- ORPHA:565779Rare disorder potentially indicated for transplant or complication after transplantation
Parents in the classifications (1):
- ORPHA:506207Rare disorder potentially indicated for transplant
rare transplant-related disorders
Children (17):
- ORPHA:85451ATTRV122I amyloidosis
- ORPHA:371176Congenital disorder of glycosylation with dilated cardiomyopathy
- ORPHA:2022Endocardial fibroelastosis
- ORPHA:300751Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
- ORPHA:154Familial isolated dilated cardiomyopathy
- ORPHA:75249Familial isolated restrictive cardiomyopathy
- ORPHA:217616Fatty acid oxidation and ketogenesis disorder with dilated cardiomyopathy
- ORPHA:367Glycogen storage disease due to glycogen branching enzyme deficiency
- ORPHA:247Inherited arrhythmogenic cardiomyopathy
- ORPHA:217638Lysosomal disease with restrictive cardiomyopathy
- ORPHA:217613Mitochondrial disease with dilated cardiomyopathy
- ORPHA:217610Neuromuscular disease with dilated cardiomyopathy
- ORPHA:324767Non-familial rare disease with dilated cardiomyopathy
- ORPHA:563Peripartum cardiomyopathy
- ORPHA:217569Rare hypertrophic cardiomyopathy
- ORPHA:217619Syndrome associated with dilated cardiomyopathy
- ORPHA:692305Triglyceride deposit cardiomyovasculopathy
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/506225
- This record as JSON: /data/d/506225.json