LP102288-0
16p11.2 chromosome region
Active
Description
16p11.2 deletion syndrome is a disorder caused by a deletion of a small piece of chromosome 16. The deletion occurs near the middle of the chromosome at a location designated p11.2. People with 16p11.2 deletion syndrome usually have developmental delay and intellectual disability. Source: National Library of Medicine, NLM
Basic Part Properties
- Part Name
- 16p11.2 chromosome region
- Part Display Name
- 16p11.2 chromosome region
- Part Type
- Component (Describes the core component or analyte measured)
- Created On
- 2010-10-07
- Construct for LOINC Short Name
- 16p11.2 chrom
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Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| zh-CN | Chinese (China) | 16p11.2 染色体区域 Synonyms: 16p11.2 染色体区域（染色体部位、 |
| es-ES | Spanish (Spain) | Deleción + duplicación de la región cromosómica 16p.11.2 |
| it-IT | Italian (Italy) | 16p.11.2, regione cromosomica",Regione cromosomica 16p.11.2,06/08/2026 23: |
| tr-TR | Turkish (Turkey) | 16p.11.2 kromozom bölgesi |
| ru-RU | Russian (Russian Federation) | 16p.11.2 хромосома участок |
| nl-NL | Dutch (Netherlands) | 16p.11.2 chromosoomgebied |
| fr-FR | French (France) | Chromosome région 16p11.2 |
| pl-PL | Polish (Poland) | Region chromosomowy 16p11.2 |
| el-GR | Greek (Greece) | Χρωμοσωμική περιοχή 16p11.2 Synonyms: Χρωμοσωμική περιοχή 16p11.2 |
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