Cardiac septal defects with coarctation of the aorta

Preferred Label : Cardiac septal defects with coarctation of the aorta;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive;

Prefixed ID : 212090;

Détails

Origin ID

212090;

UMLS CUI

C1859331;

Currated CISMeF NLP mapping
- cardiac septal defects with coarctation of the aorta [MeSH concept]
- cardiac septal defects with coarctation of the aorta [MeSH Supplementary Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Coarctation of aorta [HPO term]
- Perimembranous ventricular septal defect [HPO term]
- Secundum atrial septal defect [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- cardiac septal defects with coarctation of the aorta [MeSH Supplementary Concept]
- cardiac septal defects with coarctation of the aorta [MeSH concept]

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

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