glaucoma 3, primary congenital, D

Preferred Label : glaucoma 3, primary congenital, D;

MeSH note : mutations in LTBP2;

MeSH synonym : Glc3d;

Origin ID

C567765;

UMLS CUI

C2751316;

Currated CISMeF NLP mapping
- Glaucoma 3, primary congenital, D [OMIM Phenotype]
MeSH term(s) associated for indexing
- glaucoma [MeSH Descriptor]
Record concept(s)
- glaucoma 3, primary congenital, D [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Glaucoma 3, primary congenital, D [OMIM Phenotype]