drusen, radial, autosomal dominant

Preferred Label : drusen, radial, autosomal dominant;

Origin ID

C565088;

UMLS CUI

C1832174;

Automatic exact mappings (from CISMeF team)
- Doyne honeycomb retinal dystrophy [OMIM Phenotype]
MeSH term(s) associated for indexing
- eye diseases, hereditary [MeSH Descriptor]
- retinal drusen [MeSH Descriptor]
Record concept(s)
- drusen, radial, autosomal dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dominant drusen (disorder) [SNOMED CT concept]
- Doyne honeycomb retinal dystrophy [OMIM Phenotype]