Bifid nose - CISMeF

CISMeF

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Bifid noseMeSH concept

Preferred Label : Bifid nose;

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0529902;

UMLS CUI

C0221363;

Automatic exact mappings (from CISMeF team)
- Bifid nose, autosomal recessive [OMIM Phenotype]
Currated CISMeF NLP mapping
- Bifid nose [PASCAL descriptor]
- Bifid nose [HPO term]
- Bifid nose [ICD-11 Subcategory]
- Bifid nose [ORDO Disease]
- Bifid nose (disorder) [SNOMED CT concept]
- Midline defect of the nose [HPO term]
MeSH narrower concept(s)
- bifid nose, autosomal dominant [MeSH concept]
- bifid nose, autosomal recessive [MeSH concept]
Related record
- bifid nose [MeSH Supplementary Concept]
Semantic type(s)
- Anatomical Abnormality [UMLS semantic type]
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Bifid nose [ORDO Disease]
- Bifid nose [HPO term]
- Bifid nose (disorder) [SNOMED CT concept]
- Congenital cleft nose (disorder) [SNOMED CT concept]
- Paramedian nasal cleft [ORDO Disease]
- cleft nose [SNOMED Notion]

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27/05/2025

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