Larynx, congenital partial atresia of

Preferred Label : Larynx, congenital partial atresia of;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 150300;

Details

Origin ID

150300;

UMLS CUI

C1835555;

Automatic exact mappings (from CISMeF team)
- Larynx atresia [ORDO Disease]
Currated CISMeF NLP mapping
- larynx, congenital partial atresia of [MeSH concept]
- larynx, congenital partial atresia of [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Laryngeal obstruction [HPO term]
- Laryngeal web [HPO term]
ORDO concept(s)
- Larynx atresia [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- larynx, congenital partial atresia of [MeSH Supplementary Concept]
- larynx, congenital partial atresia of [MeSH concept]

Keyword's position in hierarchy(ies) :

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