microcephaly, retinitis pigmentosa, and sutural cataract

Preferred Label : microcephaly, retinitis pigmentosa, and sutural cataract;

Origin ID

C563296;

UMLS CUI

C1832214;

Currated CISMeF NLP mapping
- Microcephaly, retinitis pigmentosa, and sutural cataract [OMIM Phenotype]
MeSH term(s) associated for indexing
- cataract [MeSH Descriptor]
- microcephaly [MeSH Descriptor]
- retinitis pigmentosa [MeSH Descriptor]
Record concept(s)
- microcephaly, retinitis pigmentosa, and sutural cataract [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Microcephaly, retinitis pigmentosa, and sutural cataract [OMIM Phenotype]