heterotaxy, visceral, 3, autosomal

Preferred Label : heterotaxy, visceral, 3, autosomal;

Origin ID

C565237;

UMLS CUI

C1853444;

Currated CISMeF NLP mapping
- Heterotaxy, visceral, 3, autosomal [OMIM Phenotype]
MeSH term(s) associated for indexing
- heterotaxy syndrome [MeSH Descriptor]
Record concept(s)
- heterotaxy, visceral, 3, autosomal [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Heterotaxy, visceral, 3, autosomal [OMIM Phenotype]