night blindness, congenital stationary, autosomal dominant 1

Preferred Label : night blindness, congenital stationary, autosomal dominant 1;

MeSH note : mutation in rhodopsin;

MeSH synonym : night blindness, congenital stationary, Rhodopsin-Related; CSNBAD1;

Details

Origin ID

C566474;

UMLS CUI

C1864869;

Currated CISMeF NLP mapping
- Night blindness, congenital stationary, autosomal dominant 1 [OMIM Phenotype]
- congenital stationary night blindness autosomal dominant 1 [DO Concept]
MeSH term(s) associated for indexing
- eye diseases, hereditary [MeSH Descriptor]
- night blindness [MeSH Descriptor]
Record concept(s)
- night blindness, congenital stationary, autosomal dominant 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Night blindness, congenital stationary, autosomal dominant 1 [OMIM Phenotype]
- congenital stationary night blindness autosomal dominant 1 [DO Concept]

Keyword's position in hierarchy(ies) :

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