myopia 18, autosomal recessive

Preferred Label : myopia 18, autosomal recessive;

MeSH synonym : myopia 18;

Origin ID

C567606;

UMLS CUI

C2749509;

Currated CISMeF NLP mapping
- Myopia 18, autosomal recessive [OMIM Phenotype]
MeSH term(s) associated for indexing
- myopia [MeSH Descriptor]
Record concept(s)
- myopia 18, autosomal recessive [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Myopia 18, autosomal recessive [OMIM Phenotype]