omphalocele, diaphragmatic hernia, and radial ray defects

Preferred Label : omphalocele, diaphragmatic hernia, and radial ray defects;

MeSH synonym : Gershoni-Baruch syndrome;

Origin ID

C563701;

UMLS CUI

C1836007;

Automatic exact mappings (from CISMeF team)
- Omphalocele-diaphragmatic hernia-cardiovascular anomalies-radial ray defect syndrome [ORDO Disease]
Currated CISMeF NLP mapping
- Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome (disorder) [SNOMED CT concept]
- Omphalocele, diaphragmatic hernia, and radial ray defects [OMIM Phenotype]
MeSH term(s) associated for indexing
- Hernias, Diaphragmatic, Congenital [MeSH Descriptor]
- eye diseases, hereditary [MeSH Descriptor]
- hernia, diaphragmatic [MeSH Descriptor]
- hernia, umbilical [MeSH Descriptor]
Record concept(s)
- omphalocele, diaphragmatic hernia, and radial ray defects [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome (disorder) [SNOMED CT concept]
- Omphalocele, diaphragmatic hernia, and radial ray defects [OMIM Phenotype]