ORPHA:262119
Partial deletion of the long arm of chromosome 15 syndrome
Synonyms: Partial deletion of chromosome 15q · Partial monosomy of chromosome 15q · Partial monosomy of the long arm of chromosome 15
- Type
- Category
- Group
- Group of disorders
- Status
- active
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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Partial deletion of the long arm of chromosome 15 syndrome | Partial deletion of chromosome 15q · Partial monosomy of chromosome 15q · Partial monosomy of the long arm of chromosome 15 |
| fr | Syndrome de délétion partielle du bras long du chromosome 15 | Délétion partielle du chromosome 15q · Monosomie partielle du chromosome 15q · Monosomie partielle du long court du chromosome 15 |
| de | Chromosom 15q-Deletion, partielle | Chromosom 15, partielle Deletion des langen Arms · Partielle Monosomie 15q · Partielle Monosomie des langen Arms von Chromosom 15 |
| es | Síndrome de deleción parcial del brazo largo del cromosoma 15 | Deleción parcial del cromosoma 15q · Monosomía parcial del brazo largo del cromosoma 15 · Monosomía parcial del cromosoma 15q |
| it | Sindrome delezione parziale del braccio lungo del cromosoma 15 | Delezione parziale del cromosoma 15q · Monosomia parziale del braccio lungo del cromosoma 15 · Monosomia parziale del cromosoma 15q |
| nl | Partiële deletie van de lange arm van chromosoom 15-syndroom | Partiële deletie van chromosoom 15q · Partiële monosomie van chromosoom 15q · Partiële monosomie van de lange arm van chromosoom 15 |
| pt | Monossomia parcial do braço longo do cromossoma 15 | |
| pl | Zespół częściowej delecji długiego ramienia chromosomu 15 | Częściowa delecja chromosomu 15q · Cześciowa monosomia chromosomu 15q · Częściowa monosomia długiego ramienia chromosomu 15 |
| cs | Parciální delece dlouhého raménka chromozomu 15 | Parciální delece 15q · Parciální monozomie 15q · Parciální monozomie dlouhého raménka chromozomu 15 |
| uk | Часткова делеція довгого плеча хромосоми 15 | Часткова делеція хромосоми 15q · Часткова моносомія хромосоми 15q · Часткова моносомія довгого плеча хромосоми 15 |
| zh | 15号染色体长臂部分缺失 | 15号染色体长臂部分单体 |
| tr | 15. kromozomun uzun kolunun kısmi delesyonu | 15q kromozomunun kısmi delesyonu · 15q kromozomunun kısmi monozomisi · 15. kromozomun uzun kolunun kısmi monozomisi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0016913 | E | validated | |
| MONDO | 16913 | E | validated | |
| MeSH | C538038 | E | validated | |
| UMLS | C2931708 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98142Partial autosomal deletion syndrome
rare developmental anomalies during embryogenesis; rare genetic diseases
Children (8):
- ORPHA:26118315q11.2 microdeletion syndrome
- ORPHA:19931815q13.3 microdeletion syndrome
- ORPHA:9406515q24 microdeletion syndrome
- ORPHA:98794Angelman syndrome due to maternal 15q11q13 deletion
- ORPHA:261190Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion
- ORPHA:94064Deafness-infertility syndrome
- ORPHA:1596Distal deletion 15q syndrome
- ORPHA:98793Prader-Willi syndrome due to paternal 15q11q13 deletion
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/262119
- This record as JSON: /data/d/262119.json