cataract, congenital nuclear, autosomal recessive 1

Preferred Label : cataract, congenital nuclear, autosomal recessive 1;

MeSH synonym : CATCN1;

Origin ID

C563728;

UMLS CUI

C1836272;

Currated CISMeF NLP mapping
- Cataract 35 [OMIM Phenotype]
- cataract 35 [DO Concept]
MeSH term(s) associated for indexing
- cataract [MeSH Descriptor]
- eye diseases, hereditary [MeSH Descriptor]
Record concept(s)
- cataract, congenital nuclear, autosomal recessive 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cataract 35 [OMIM Phenotype]
- cataract 35 [DO Concept]