stargardt disease 3

Preferred Label : stargardt disease 3;

MeSH synonym : macular dystrophy with flecks, type 3; macular dystrophy, autosomal dominant, chromosome 6-linked,; Stargardt-Like macular dystrophy, autosomal dominant;

Details

Origin ID

C535805;

UMLS CUI

C1838644;

Currated CISMeF NLP mapping
- Stargardt disease 3 [OMIM Phenotype]
MeSH term(s) associated for indexing
- macular degeneration [MeSH Descriptor]
Record concept(s)
- Stargardt disease 3 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Stargardt disease 3 [OMIM Phenotype]

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