cataract, congenital nuclear, autosomal recessive 3

Preferred Label : cataract, congenital nuclear, autosomal recessive 3;

MeSH synonym : CATCN3;

Origin ID

C566923;

UMLS CUI

C1969062;

Currated CISMeF NLP mapping
- Cataract 17, multiple types [OMIM Phenotype]
- cataract 17 multiple types [DO Concept]
MeSH term(s) associated for indexing
- cataract [MeSH Descriptor]
- eye diseases, hereditary [MeSH Descriptor]
Record concept(s)
- cataract, congenital nuclear, autosomal recessive 3 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]