ORPHA:309568
Defect in conserved oligomeric Golgi complex
Synonyms: Defect in COG complex
- 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 | Defect in conserved oligomeric Golgi complex | Defect in COG complex |
| fr | Anomalie du complexe oligomérique du Golgi | Anomalie de COG |
| de | Störung des konservierten oligomeren Golgi-Komplex | COG-Komplex-Defekt |
| es | Defecto en el complejo oligomérico conservado de Golgi | Defecto en el complejo COG |
| it | Difetto del complesso oligomerico conservato del Golgi | Difetto di COG |
| nl | Defect in geconserveerd oligomeer Golgi-complex | Defect in COG-complex |
| pt | Defeito no complexo de Golgi oligomérico conservado | |
| pl | Wady zachowanego oligomerycznego aparatu Golgiego | Wada kompleksu COG |
| cs | Defekty v konzervovaném oligomerickém Golgiho komplexu | Defekty v COG komplexu |
| uk | Дефект у консервативному олігомерному комплексі Гольджі | Дефект в COG комплексі |
| zh | 保守寡聚高尔基复合体缺陷 | COG复合体缺陷 |
| tr | Korunan oligomerik Golgi kompleksi defekti | COG kompleksinde defekt |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0017750 | E | validated | |
| MONDO | 17750 | E | validated | |
| UMLS | C5679953 | 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:309526Disorder of multiple glycosylation
rare inborn errors of metabolism; rare genetic diseases
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/309568
- This record as JSON: /data/d/309568.json