microcephaly, congenital heart disease, unilateral renal agenesis, and hyposegmented lungs

Preferred Label : microcephaly, congenital heart disease, unilateral renal agenesis, and hyposegmented lungs;

Origin ID

C563341;

UMLS CUI

C1832436;

Automatic exact mappings (from CISMeF team)
- Microcephaly, congenital heart disease, unilateral renal agenesis, and hyposegmented lungs [OMIM Phenotype]
MeSH term(s) associated for indexing
- heart defects, congenital [MeSH Descriptor]
- kidney [MeSH Descriptor]
- lung [MeSH Descriptor]
- microcephaly [MeSH Descriptor]
Record concept(s)
- microcephaly, congenital heart disease, unilateral renal agenesis, and hyposegmented lungs [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Microcephaly, congenital heart disease, unilateral renal agenesis, and hyposegmented lungs [OMIM Phenotype]