lymphedema, hereditary, IB

Preferred Label : lymphedema, hereditary, IB;

MeSH synonym : LMPH1B;

Origin ID

C567452;

UMLS CUI

C2677787;

Currated CISMeF NLP mapping
- Lymphatic malformation 2 [OMIM Phenotype]
- hereditary lymphedema IB [DO Concept]
MeSH term(s) associated for indexing
- lymphedema [MeSH Descriptor]
Record concept(s)
- lymphedema, hereditary, IB [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Lymphatic malformation 2 [OMIM Phenotype]