caudal duplication anomaly

Preferred Label : caudal duplication anomaly;

MeSH note : associated with hypermethylation of the AXIN1 promoter;

Origin ID

C564315;

UMLS CUI

C1842884;

Currated CISMeF NLP mapping
- Caudal duplication [ICD-11 More detail]
- Caudal duplication [ORDO Disease]
- Caudal duplication anomaly [OMIM Phenotype]
MeSH term(s) associated for indexing
- congenital abnormalities [MeSH Descriptor]
Record concept(s)
- caudal duplication anomaly [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Caudal duplication [ORDO Disease]
- Caudal duplication anomaly [OMIM Phenotype]