ORPHA:1611
OBSOLETE: Deletion 20p
inactive · referred to ORPHA:261992Partial deletion of the short arm of chromosome 20 syndrome
Synonyms: OBSOLETE: Monosomy 20p
- 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 Partial deletion of the short arm of chromosome 20
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Deletion 20p | OBSOLETE: Monosomy 20p |
| fr | OBSOLETE : Délétion 20p | OBSOLETE : Monosomie 20p |
| de | OBSOLET: Deletion 20p | OBSOLET: Monosomie 20p |
| es | OBSOLETO: Deleción 20p | OBSOLETO: Monosomía 20p |
| it | OBSOLETO: Delezione 20p | OBSOLETO: Monosomia 20p |
| nl | OBSOLEET: Deletie 20p | OBSOLEET: Monosomie 20p |
| pt | OBSOLETO: Deleção 20p | OBSOLETO: Monossomia 20p |
| pl | NIEAKTUALNE: Delecja 20p | NIEAKTUALNE: Monosomia 20p |
| cs | NEAKTUÁLNÍ: Deletion 20p | = en |
| uk | ЗАСТАРІЛО: Делеція 20p | ЗАСТАРІЛО: Моносомія 20р |
| zh | 弃用：20号染色体短臂缺失 | 20号染色体短臂单体 |
| tr | Eski adı: Delesyon 20p | Monozomi 20p |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
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.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/1611
- This record as JSON: /data/d/1611.json