Retinoschisis, Autosomal Dominant

Preferred Label : Retinoschisis, Autosomal Dominant;

MeSH synonym : Retinoschisis autosomal dominant; Autosomal dominant retinoschisis;

Origin ID

C000598640;

UMLS CUI

C1867235;

Currated CISMeF NLP mapping
- Retinoschisis, autosomal dominant [OMIM Phenotype]
MeSH term(s) associated for indexing
- retinoschisis [MeSH Descriptor]
Record concept(s)
- Retinoschisis, Autosomal Dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Retinoschisis, autosomal dominant [OMIM Phenotype]