ORPHA:695032
Giant omphalocele
Synonyms: Major omphalocele
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Giant omphalocele | Major omphalocele |
| fr | Omphalocèle géante | Hépatocèle · Omphalocèle de grande taille |
| de | Riesen-Omphalozele | Große Omphalozele · Omphalozele major |
| es | Onfalocele gigante | Onfalocele mayor |
| it | Onfalocele gigante | Onfalocele maggiore |
| nl | Grote omfalocele | |
| pt | Giant omphalocele | |
| pl | Giant omphalocele | = en |
| cs | Giant omphalocele | = en |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:660Omphalocele
rare developmental anomalies during embryogenesis; rare abdominal surgical diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
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/695032
- This record as JSON: /data/d/695032.json