ORPHA:139006
OBSOLETE: Sequence or association
inactive · referred to ORPHA:93890Rare developmental defect during embryogenesis
- 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 developmental defect during embryogenesis
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Sequence or association | |
| fr | OBSOLETE : Séquence ou association | |
| de | OBSOLET: Sequenz oder Assoziation | |
| es | OBSOLETO: Secuencia o asociación | |
| it | OBSOLETO: Sequenza o associazione | |
| nl | OBSOLEET: Sequentie of associatie | |
| pt | OBSOLETO: Sequência ou associação | |
| pl | NIEAKTUALNE: Sekwencja/asocjacja | |
| cs | NEAKTUÁLNÍ: Sekvence nebo asociace | |
| uk | ЗАСТАРІЛО: Послідовність або асоціація | |
| zh | 弃用：序列或关联 | |
| tr | Eski adı: Dizi veya ilişkilendirme |
2
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.
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/139006
- This record as JSON: /data/d/139006.json