edinburgh malformation syndrome

Preferred Label : edinburgh malformation syndrome;

Origin ID

C563051;

UMLS CUI

C0795933;

Currated CISMeF NLP mapping
- Edinburgh malformation syndrome [OMIM Phenotype]
- Edinburgh malformation syndrome [ORDO Disease]
- Edinburgh malformation syndrome (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- chromosome aberrations [MeSH Descriptor]
- chromosome disorders [MeSH Descriptor]
- facies [MeSH Descriptor]
- failure to thrive [MeSH Descriptor]
- hydrocephalus [MeSH Descriptor]
- psychomotor disorders [MeSH Descriptor]
Record concept(s)
- edinburgh malformation syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Edinburgh malformation syndrome [OMIM Phenotype]
- Edinburgh malformation syndrome [ORDO Disease]
- Edinburgh malformation syndrome (disorder) [SNOMED CT concept]