Cone-Rod dystrophy 13

Preferred Label : Cone-Rod dystrophy 13;

MeSH note : mutation in RPGRIP1;

MeSH synonym : CORD13;

Origin ID

C567698;

UMLS CUI

C2750720;

Currated CISMeF NLP mapping
- Cone-rod dystrophy 13 [OMIM Phenotype]
- cone-rod dystrophy 13 [DO Concept]
MeSH term(s) associated for indexing
- retinitis pigmentosa [MeSH Descriptor]
Record concept(s)
- Cone-Rod dystrophy 13 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cone-rod dystrophy 13 [OMIM Phenotype]
- cone-rod dystrophy 13 [DO Concept]