Bifid nose, autosomal recessive

Preferred Label : Bifid nose, autosomal recessive;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Nose, median cleft of; Median fissure of nose;

Inheritance : Autosomal recessive;

Prefixed ID : 210400;

Details

Origin ID

210400;

UMLS CUI

C3887497;

Automatic exact mappings (from CISMeF team)
- Bifid nose [MeSH concept]
- bifid nose [MeSH Supplementary Concept]
Broader ORDO disease(s)
- Bifid nose [ORDO Disease]
Currated CISMeF NLP mapping
- bifid nose, autosomal recessive [MeSH concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Bifid nose [HPO term]
- Midline defect of the nose [HPO term]
ORDO concept(s)
- Bifid nose [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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