Cone-Rod dystrophy, X-Linked, 3

Preferred Label : Cone-Rod dystrophy, X-Linked, 3;

MeSH note : mutation in CACNA1F;

MeSH synonym : CORDX3;

Origin ID

C564507;

UMLS CUI

C1845407;

Currated CISMeF NLP mapping
- Cone-rod dystrophy, X-linked, 3 [OMIM Phenotype]
- X-linked cone-rod dystrophy 3 [DO Concept]
MeSH term(s) associated for indexing
- genetic diseases, X-linked [MeSH Descriptor]
- retinitis pigmentosa [MeSH Descriptor]
Record concept(s)
- Cone-Rod dystrophy, X-Linked, 3 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cone-rod dystrophy, X-linked, 3 [OMIM Phenotype]
- X-linked cone-rod dystrophy 3 [DO Concept]