cataract, autosomal dominant, multiple types 1

Preferred Label : cataract, autosomal dominant, multiple types 1;

MeSH note : mutation on phakinin;

Origin ID

C566909;

UMLS CUI

C1969032;

Currated CISMeF NLP mapping
- Cataract 12, multiple types [OMIM Phenotype]
MeSH term(s) associated for indexing
- cataract [MeSH Descriptor]
Record concept(s)
- cataract, autosomal dominant, multiple types 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]