cataract, congenital nuclear, autosomal recessive 2

Preferred Label : cataract, congenital nuclear, autosomal recessive 2;

MeSH synonym : CATCN2;

Origin ID

C565725;

UMLS CUI

C1857853;

Currated CISMeF NLP mapping
- Cataract 22, multiple types [OMIM Phenotype]
- cataract 22 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 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cataract 22, multiple types [OMIM Phenotype]