ORPHA:692296
Idiopathic triglyceride deposit cardiomyovasculopathy
Synonyms: I-TGCV · Idiopathic neutral lipid storage disease with severe cardiovascular involvement
- Type
- Etiological subtype
- Group
- Subtype of disorder
- Inheritance
- Unknown
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Idiopathic triglyceride deposit cardiomyovasculopathy | I-TGCV · Idiopathic neutral lipid storage disease with severe cardiovascular involvement |
| fr | Cardiomyovasculopathie idiopathique à surcharge lipidique | I-TGCV · Maladie à surcharge lipidique avec atteinte cardiovasculaire idiopathique sévère |
| de | Triglycerid-Speicher-Kardiomyovaskulopathie, idiopathische | I-TGCV · Idiopathische Neutralfett-Speicherkrankheit mit schwerer kardiovaskulärer Beteiligung |
| es | Vasculopatía miocárdica por depósito de triglicéridos idiopática | Enfermedad por depósito de lípidos neutros con afectación cardiovascular grave idiopática · I-TGCV |
| it | Cardiomiovasculopatia idiopatica da depositi di trigliceridi | I-TGCV · Malattia idiopatica da accumulo di lipidi neutri con grave coinvolgimento cardiovascolare |
| nl | Idiopathische cardiomyovasculopathie met depositie van triglyceriden | I-TGCV · Idiopathische neutrale lipidestapelingsziekte met ernstige cardiovasculaire betrokkenheid |
| pt | Cardiomiovasculopatia idiopática por depósito de triglicéridos | Doença idiopática de armazenamento de lípidos neutros com envolvimento cardiovascular grave · I-TGCV |
| pl | Idiopatyczna kardiomiowaskulopatia z odkładaniem złogów triglicerydów | = en |
| cs | Idiopatická kardiomyovaskulopatie s triglyceridovými ložisky | = en |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:692305Triglyceride deposit cardiomyovasculopathy
rare cardiac diseases; rare inborn errors of metabolism; rare genetic diseases; rare neurological diseases; rare transplant-related disorders
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/692296
- This record as JSON: /data/d/692296.json