ORPHA:464682
OBSOLETE: Disorder with acute infantile liver failure
inactive · referred to ORPHA:101939Rare parenchymal liver disease
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Rare parenchymal liver disease
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Disorder with acute infantile liver failure | |
| fr | OBSOLETE : Maladie avec insuffisance hépatique aigu infantile | |
| de | OBSOLET: Krankheit mit akutem infantilen Leberversagen | |
| es | OBSOLETO: Trastorno con insuficiencia hepática aguda infantil | |
| it | OBSOLETO: Disorder with acute infantile liver failure | |
| nl | OBSOLEET: Aandoening met acuut infantiel leverfalen | |
| pt | OBSOLETO: Doença com insuficiência hepática aguda da infância | |
| pl | NIEAKTUALNE: Zaburzenia z ostra niewydolnoscia watroby u niemowlat | |
| cs | NEAKTUÁLNÍ: Porucha s akutním dětským selháním jater | |
| uk | ЗАСТАРІЛО: Захворювання з гострою дитячою печінковою недостатністю | |
| zh | 已废除：急性婴儿肝衰竭相关疾病 | |
| tr | Eski adı: Akut infantil karaciğer yetmezliği ile seyreden bozukluk |
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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/464682
- This record as JSON: /data/d/464682.json