Omphalocele, diaphragmatic hernia, and radial ray defects

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

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Gershoni-baruch syndrome;

Prefixed ID : 609545;

Details

Origin ID

609545;

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 [MeSH concept]
- omphalocele, diaphragmatic hernia, and radial ray defects [MeSH Supplementary Concept]
ORDO concept(s)
- Omphalocele-diaphragmatic hernia-cardiovascular anomalies-radial ray defect syndrome [ORDO Disease]
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 [MeSH Supplementary Concept]
- omphalocele, diaphragmatic hernia, and radial ray defects [MeSH concept]

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