ORPHA:96152
OBSOLETE: Distal monosomy 20q
inactive · referred to ORPHA:26131120q13.33 microdeletion syndrome
Synonyms: OBSOLETE: Distal deletion 20q · OBSOLETE: Monosomy 20qter · OBSOLETE: Telomeric deletion 20q
- 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 20q13.33 microdeletion syndrome
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Distal monosomy 20q | OBSOLETE: Distal deletion 20q · OBSOLETE: Monosomy 20qter · OBSOLETE: Telomeric deletion 20q |
| fr | OBSOLETE : Monosomie distale 20q | OBSOLETE : Délétion distale 20p · OBSOLETE : Délétion télomérique 20q · OBSOLETE : Monosomie 20qter |
| de | OBSOLET: Monosomie 20q, distale | OBSOLET: Monosomie 20qter · OBSOLET: Deletion 20q, distale |
| es | OBSOLETO: Monosomía terminal 20q | OBSOLETO: Deleción telomérica 20q · OBSOLETO: Deleción terminal 20q · OBSOLETO: Monosomía 20qter |
| it | OBSOLETO: Monosomia distale 20q | OBSOLETO: Delezione 20q distale · OBSOLETO: Delezione 20q telomerica · OBSOLETO: Monosomia 20qter |
| nl | OBSOLEET: Distale monosomie 20q | OBSOLEET: Distale deletie 20q · OBSOLEET: Monosomie 20qter · OBSOLEET: Telomerische deletie 20q |
| pt | OBSOLETO: Monossomia distal 20q | OBSOLETO: Deleção distal 20q · OBSOLETO: Monossomia 20qter |
| pl | NIEAKTUALNE: Dystalna monosomia 20q | NIEAKTUALNE: Delecja dystalna 20q · NIEAKTUALNE: Delecja telomerowa 20q · NIEAKTUALNE: Monosomia 20qter |
| cs | NEAKTUÁLNÍ: Distální monozomie 20q | NEAKTUÁLNÍ: Distální delece 20q · NEAKTUÁLNÍ: Monozomie 20qter · NEAKTUÁLNÍ: Telomerická delece 20q |
| uk | ЗАСТАРІЛО: Дистальна моносомія 20q | ЗАСТАРІЛО: Дистальна делеція 20q · ЗАСТАРІЛО: Моносомія 20qter · ЗАСТАРІЛО: Делеція теломерної ділянки 20q |
| zh | 20号染色体长臂远端单体 | 20号染色体长臂端粒缺失 |
| tr | Distal monozomi 20q | Monozomi 20qter · Distal delesyon 20q · Telomerik delesyon 20q |
Definition in:
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.
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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/96152
- This record as JSON: /data/d/96152.json