Hirschsprung disease with heart defects, laryngeal anomalies, and preaxial polydactyly

Preferred Label : Hirschsprung disease with heart defects, laryngeal anomalies, and preaxial polydactyly;

Type : Other, mainly phenotypes with suspected mendelian basis;

Prefixed ID : 604211;

Détails

Origin ID

604211;

UMLS CUI

C1858696;

Automatic exact mappings (from CISMeF team)
- hirschsprung disease with heart defects, laryngeal anomalies, and preaxial polydactyly [MeSH Supplementary Concept]
- hirschsprung disease with heart defects, laryngeal anomalies, and preaxial polydactyly [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- hirschsprung disease with heart defects, laryngeal anomalies, and preaxial polydactyly [MeSH Supplementary Concept]
- hirschsprung disease with heart defects, laryngeal anomalies, and preaxial polydactyly [MeSH concept]

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

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