ORPHA:98711
OBSOLETE: Metabolic disease with corneal opacity
inactive · referred to ORPHA:68367Rare inborn error of metabolism
- 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 inborn errors of metabolism
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Metabolic disease with corneal opacity | |
| fr | OBSOLETE : Maladie métabolique avec opacité cornéenne | |
| de | OBSOLET: Stoffwechselkrankheit mit Hornhauttrübung | |
| es | OBSOLETO: Enfermedad metabólica con opacidad córnea | |
| it | OBSOLETO: Malattia metabolica associata a opacità corneale | |
| nl | OBSOLEET: Stofwisselingsziekte met opaciteit van cornea | OBSOLEET: Metabole aandoening met hoornvliestroebeling |
| pt | OBSOLETO: Doença metabólica com opacidade da córnea | |
| pl | NIEAKTUALNE: Choroba metaboliczna ze zmetnieniem rogówki | |
| cs | NEAKTUÁLNÍ: Metabolická onemocnění s korneální opacitou | |
| uk | ЗАСТАРІЛО: Метаболічне захворювання з помутнінням рогівки | |
| zh | 弃用：角膜混浊代谢性疾病 | |
| tr | Eski adı: Korneal opasite ile seyreden metabolik hastalık |
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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/98711
- This record as JSON: /data/d/98711.json