Cone-Rod dystrophy 12

Preferred Label : Cone-Rod dystrophy 12;

MeSH note : mutation in PROM1;

MeSH synonym : CORD12;

Origin ID

C567206;

UMLS CUI

C2675210;

Currated CISMeF NLP mapping
- Cone-rod dystrophy 12 [OMIM Phenotype]
- cone-rod dystrophy 12 [DO Concept]
MeSH term(s) associated for indexing
- retinitis pigmentosa [MeSH Descriptor]
Record concept(s)
- Cone-Rod dystrophy 12 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cone-rod dystrophy 12 [OMIM Phenotype]
- cone-rod dystrophy 12 [DO Concept]