polycystic kidney, cataract, and congenital blindness

Preferred Label : polycystic kidney, cataract, and congenital blindness;

Origin ID

C564882;

UMLS CUI

C1849771;

Currated CISMeF NLP mapping
- Polycystic kidney, cataract, and congenital blindness [OMIM Phenotype]
MeSH term(s) associated for indexing
- blindness [MeSH Descriptor]
- cataract [MeSH Descriptor]
- polycystic kidney diseases [MeSH Descriptor]
Record concept(s)
- polycystic kidney, cataract, and congenital blindness [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Polycystic kidney, cataract, and congenital blindness [OMIM Phenotype]