ORPHA:209047
Qualitative or quantitative defects of filamin C
- 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 | Qualitative or quantitative defects of filamin C | |
| fr | Anomalie qualitative ou quantitative de la filamine C | |
| de | Filamin C, qualitative oder quantitative Defekte | |
| es | Anomalías cualitativas o cuantitativas de filamina C | |
| it | Alterazioni qualitative o quantitative di filamina C | |
| nl | Kwalitatieve of kwantitatieve defecten van filamine C | |
| pt | Deficiências qualitativas e quantitativas de filamina C | |
| pl | Defekty jakościowe lub ilościowe filaminy C | |
| cs | Kvalitativní nebo kvantitativní defekty filaminu C | |
| uk | Якісні або кількісні дефекти філаміну С | |
| zh | 细丝蛋白C定性或定量缺陷 | |
| tr | C filamininin kalitatif veya kantitatif defekti |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0016189 | E | validated | |
| MONDO | 16189 | E | validated | |
| UMLS | C5680841 | 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:209038Qualitative or quantitative defects of myofibrillar proteins
rare genetic diseases
Children (1):
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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/209047
- This record as JSON: /data/d/209047.json