ORPHA:70474
Leigh syndrome with cardiomyopathy
inactive · moved to ORPHA:506Leigh syndrome
Synonyms: Cardiomyopathy with hypotonia due to cytochrome C oxidase deficiency · Cardiomyopathy with myopathy due to COX deficiency · Leigh disease with myopathy
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Leigh syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Leigh syndrome with cardiomyopathy | Cardiomyopathy with hypotonia due to cytochrome C oxidase deficiency · Cardiomyopathy with myopathy due to COX deficiency · Leigh disease with myopathy |
| fr | Syndrome de Leigh avec cardiomyopathie | Cardiomyopathie avec hypotonie par déficit en cytochrome C oxydase · Cardiomyopathie avec myopathie par déficit en COX · Maladie de Leigh avec myopathie |
| de | Leigh-Syndrom - Kardiomyopathie | Kardiomyopathie mit Hypotonie durch Cytochrome-C-Oxidase-Mangel · Kardiomyopathie mit Myopathie durch COX-Mangel · Leigh-Syndrom mit Myopathie |
| es | Síndrome de Leigh con miocardiopatía | Cardiomiopatía con hipotonía por deficiencia de citocromo C oxidasa · Enfermedad de Leigh con miopatía · Miocardiopatía con hipotonía por deficiencia de citocromo C oxidasa · Miocardiopatía con miopatía por deficiencia de COX |
| it | Sindrome di Leigh con cardiomiopatia | Cardiomiopatia con ipotonia da deficit di citocromo C ossidasi · Cardiomiopatia con miopatia da deficit di COX · Malattia di Leigh con miopatia |
| nl | Syndroom van Leigh met cardiomyopathie | Cardiomyopathie met hypotonie als gevolg van cytochroom C-oxidasedeficiëntie · Cardiomyopathie met myopathie als gevolg van COX-deficiëntie · Ziekte van Leigh met myopathie |
| pt | Síndrome Leigh com miocardiopatia | Miocardiopatia com hipotonia por deficiência de citocromo C oxidase · Miocardiopatia com miopatia por deficiência de COX |
| pl | Zespół Leigha z kardiomiopatią | Choroba Leigha z miopatią · Kardiomiopatia z hipotonią spowodowana niedoborem oksydazy cytochromu C · Kardiomiopatia z miopatią spowodowana niedoborem COX |
| cs | Leighův syndrom s kardiomyopatií | Leighova choroba s myopatií · Kardiomyopatie s hypotonií na podkladě deficitu cytochrom C oxidázy · Kardiomyopatie s myopatií na podkladě deficitu COX |
| uk | Синдром Лі з кардіоміопатією | Кардіоміопатія з гіпотензією внаслідок дефіциту цитохрому С оксидази · Кардіоміопатія з міопатією внаслідок дефіциту COX · Хвороба Лі з міопатією |
| zh | 利氏综合征伴心肌病 | 细胞色素C氧化酶缺乏所致心肌病伴发肌病 |
| tr | Kardiyomiyopati ile seyreden Leigh sendromu | Miyopatili Leigh hastalığı · COX eksikliğine bağlı miyopatili kardiyomiyopati · Sitokrom C oksidaz eksikliğine bağlı hipotoni ile seyreden kardiyomiyopati |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680116 | 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
Not placed in any Orphanet classification in this release.
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/70474
- This record as JSON: /data/d/70474.json