Cleft larynx, posterior

Preferred Label : Cleft larynx, posterior;

Type : Other, mainly phenotypes with suspected mendelian basis;

Included titles and symbols : Stridor, congenital;

Inheritance : ? Autosomal recessive;

Prefixed ID : 215800;

Détails

Origin ID

215800;

UMLS CUI

C1859083;

Automatic exact mappings (from CISMeF team)
- Congenital stridor [MedDRA LLT]
- Laryngotracheoesophageal cleft [ORDO Disease]
- laryngeal cleft [MeSH Supplementary Concept]
- stridor, congenital [MeSH concept]
- stridor, congenital [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- Laryngo-tracheo-esophageal cleft-pulmonary hypoplasia syndrome [ORDO Disease]
- Novak syndrome [MeSH concept]
- novak syndrome [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of the voice [HPO term]
- Aspiration [HPO term]
- Autosomal recessive inheritance [HPO term]
- Cyanosis [HPO term]
- Laryngeal stridor [HPO term]
ORDO concept(s)
- Laryngotracheoesophageal cleft [ORDO Disease]
- Laryngotracheoesophageal cleft type 3 [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Laryngo-tracheo-esophageal cleft-pulmonary hypoplasia syndrome [ORDO Disease]
- Novak syndrome [MeSH concept]
- novak syndrome [MeSH Supplementary Concept]

Position du mot-clé dans l'(les) arborescence(s) :

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