Preferred Label : Hirschsprung disease with heart defects, laryngeal anomalies, and preaxial polydactyly;
Type : Other, mainly phenotypes with suspected mendelian basis;
Prefixed ID : 604211;
Origin ID : 604211;
UMLS CUI : C1858696;
Automatic exact mappings (from CISMeF team)
Semantic type(s)
UMLS correspondences (same concept)