retinal cone dystrophy 2

Preferred Label : retinal cone dystrophy 2;

MeSH synonym : cone degeneration, autosomal dominant progressive; Cone-Rod dystrophy 6;

Origin ID

C538363;

UMLS CUI

C1866293;

Automatic exact mappings (from CISMeF team)
- cone-rod dystrophy 6 [DO Concept]
MeSH term(s) associated for indexing
- retinitis pigmentosa [MeSH Descriptor]
Record concept(s)
- Retinal cone dystrophy 2 [MeSH concept]
See also inter- (CISMeF)
- Cone-rod dystrophy 6 [OMIM Phenotype]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cone-rod dystrophy 6 [OMIM Phenotype]
- cone-rod dystrophy 6 [DO Concept]