Other congenital malformations of nose

Preferred Label : Other congenital malformations of nose;

Inclusion CIM-10 : Congenital anomaly of nasal sinus wall; Accessory nose;

Associé à un acte opératoire (%) : 85.0;

Diag associé à un acte (%) : 97.8;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q308;

UMLS CUI

C0478014;

Automatic exact mappings (from CISMeF team)
- Accessory nose (disorder) [SNOMED CT concept]
- Polyrrhinia [ICD-11 More detail]
Orphanet concepts
- Congenital nasal pyriform aperture stenosis with holoprosencephaly [ORDO Disease]
- Craniorhiny [ORDO Disease]
- Familial nasal acilia [ORDO Disease]
- Isolated congenital nasal pyriform aperture stenosis [ORDO Disease]
- Nasal glial heterotopia [ORDO Disease]
- Nose and cavum anomaly [ORDO Disease]
- Polyrrhinia [ORDO Disease]
- Proboscis lateralis [ORDO Disease]
- Supernumerary nostril [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Other anomalies of nose [ICD-9 code]

Keyword's position in hierarchy(ies) :

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