ORPHA:2129
OBSOLETE: Hemihypertrophy-intestinal web-corneal opacity syndrome
inactive · referred to ORPHA:102285Multiple congenital anomalies/dysmorphic syndrome without intellectual disability
Synonyms: OBSOLETE: HIPO syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Multiple congenital anomalies/dysmorphic syndrome without intellectual disability
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Hemihypertrophy-intestinal web-corneal opacity syndrome | OBSOLETE: HIPO syndrome |
| fr | OBSOLETE : Syndrome d'hémihypertrophie-bride intestinale-opacités cornéennes | OBSOLETE : Syndrome HIPO |
| de | OBSOLET: Hemihypertrophie-intestinales Netz-Hornhauttrübung-Syndrom | OBSOLET: HIPO-Syndrom |
| es | OBSOLETO: Síndrome de hemihipertrofia-brida intestinal-opacidad corneal | OBSOLETO: Síndrome de HIPO |
| it | OBSOLETO: emi-ipertrofia-briglia intestinale-opacità corneali | OBSOLETO: Sindrome HIPO |
| nl | OBSOLEET: Hemihypertrofie - intestinaal web - corneale opaciteit-syndroom | OBSOLEET: HIPO-syndroom |
| pt | OBSOLETO: Síndrome de hemihipertrofia-teia intestinal-opacidade da córnea | OBSOLETO: Síndrome HIPO |
| pl | NIEAKTUALNE: Przerost polowiczy - siec jelitowa - zmetnienie rogówki | NIEAKTUALNE: Zespół HIPO |
| cs | NEAKTUÁLNÍ: Syndrom hemihypertrofie, atrézie střeva a katarakty | = en |
| uk | ЗАСТАРІЛО: Синдром гемігіпертрофії-перетинки кишечнику-помутніння рогівки | ЗАСТАРІЛО: Синдром HIPO |
| zh | 偏侧发育过度-肠道粘连-角膜斑综合征 | HIPO综合征 |
| tr | Eski adı: Hemihipertrofi-bağırsak ağ-korneal opasite sendromu | HIPO sendromu |
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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/2129
- This record as JSON: /data/d/2129.json