ORPHA:717646
Congenital midnasal stenosis
Synonyms: CMNS
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital midnasal stenosis | CMNS |
| fr | Sténose congénitale nasale médiale | |
| de | Kongenitale midnasale Stenose | = en |
| es | Estenosis medionasal congénita | |
| it | Stenosi nasale media congenita | = en |
| nl | Congenitale midnasale stenose | CMNS · Congenitale midnasale vernauwing |
| pt | Congenital midnasal stenosis | |
| pl | Wrodzone zwężenie środkowego odcinka nosa | = en |
| cs | Congenital midnasal stenosis | = en |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:156246Nose and cavum anomaly
rare developmental anomalies during embryogenesis; rare otorhinolaryngological diseases
No children.
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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/717646
- This record as JSON: /data/d/717646.json