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

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

Origin ID

C565817;

UMLS CUI

C1858696;

Automatic exact mappings (from CISMeF team)
- Hirschsprung disease with heart defects, laryngeal anomalies, and preaxial polydactyly [OMIM Phenotype]
MeSH term(s) associated for indexing
- abnormalities, multiple [MeSH Descriptor]
- heart defects, congenital [MeSH Descriptor]
- hirschsprung disease [MeSH Descriptor]
- larynx [MeSH Descriptor]
- polydactyly [MeSH Descriptor]
Record concept(s)
- 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 [OMIM Phenotype]