trisomy 18-Like syndrome

Preferred Label : trisomy 18-Like syndrome;

Origin ID

C563382;

UMLS CUI

C1832677;

Currated CISMeF NLP mapping
- Trisomy 18-like syndrome [OMIM Phenotype]
MeSH term(s) associated for indexing
- abnormalities, multiple [MeSH Descriptor]
- chromosome disorders [MeSH Descriptor]
- chromosomes, human, pair 18 [MeSH Descriptor]
- trisomy [MeSH Descriptor]
Record concept(s)
- trisomy 18-Like syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Trisomy 18-like syndrome [OMIM Phenotype]