ORPHA:209188
Qualitative or quantitative defects of emerin
- 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 emerin | |
| fr | Anomalie qualitative ou quantitative de l'émerine | |
| de | Emerin, qualitative oder quantitative Defekte | |
| es | Anomalías cualitativas o cuantitativas de la emerina | |
| it | Difetti qualitativi o quantitativi dell'emerina | Emerinopatia |
| nl | Kwalitatieve of kwantitatieve defecten van emerine | |
| pt | Deficiências qualitativas e quantitativas de emerina | |
| pl | Defekty jakościowe lub ilościowe emeryny | |
| cs | Kvalitativní nebo kvantitativní defekty emerinu | |
| uk | Якісні або кількісні дефекти емерину | |
| zh | 伊默菌素定性或定量缺陷 | |
| tr | Emerin kalitatif veya kantitatif defekti |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16196 | E | validated | |
| UMLS | C5680833 | 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:207049Qualitative or quantitative protein defects in neuromuscular diseases
rare genetic diseases
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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/209188
- This record as JSON: /data/d/209188.json