ORPHA:156156
Lipoatrophy with diabetes, leukomelanodermic papules, liver steatosis, and hypertrophic cardiomyopathy
inactive · moved to ORPHA:79474Atypical Werner syndrome
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Atypical Werner syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Lipoatrophy with diabetes, leukomelanodermic papules, liver steatosis, and hypertrophic cardiomyopathy | |
| fr | Lipoatrophie avec diabète, papules leucomélanodermiques, stéatose hépatique et cardiomyopathie hypertrophique | |
| de | Lipoatrophie mit Diabetes - leukomelanodermale Papeln - Lebersteatose - hypertrophe Kardiomyopathie | |
| es | Lipoatrofia con diabetes, pápulas leucomelanodérmicas, esteatosis hepática y miocardiopatía hipertrófica | |
| it | Lipoatrofia con diabete, papule leucomelanodermiche, steatosi epatica e cardiomiopatia ipertrofica | |
| nl | Lipoatrofie met diabetes, leukomelanodermale papels, leversteatose en hypertrofische cardiomyopathie | |
| pt | Lipoatrofia com diabetes, pápulas leucomelanodérmicas, esteatose hepática e miocardiopatia hipertrófica | |
| pl | Zanik tkanki tłuszczowej z cukrzycą, grudkami leukomelanotycznymi, zwyrodnieniem tłyszczowym wątroby i kardiomiopatią przerostową | |
| cs | Lipoatrofie s diabetem, leukomelanodermickými papulami, steatózou jater a hypertrofickou kardiomyopatií | |
| uk | Ліпоатрофія з діабетом, лейкомеланодермальними папулами, стеатозом печінки та гіпертрофічною кардіоміопатією | |
| zh | 脂肪萎缩伴糖尿病、白斑丘疹、肝脂肪变性和肥厚型心肌病 | |
| tr | Diyabet, lökomelanodermik papüller, karaciğer steatozu ve hipertrofik kardiyomiyopati ile seyreden lipoatrofi |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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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/156156
- This record as JSON: /data/d/156156.json