retinal nonattachment and falciform detachment

Preferred Label : retinal nonattachment and falciform detachment;

Origin ID

C566717;

UMLS CUI

C1867315;

Automatic exact mappings (from CISMeF team)
- Persistent hyperplastic primary vitreous, autosomal recessive [OMIM Phenotype]
Currated CISMeF NLP mapping
- Retinal nonattachment and falciform detachment [OMIM Phenotype]
MeSH term(s) associated for indexing
- retina [MeSH Descriptor]
- retinal detachment [MeSH Descriptor]
Record concept(s)
- retinal nonattachment and falciform detachment [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Retinal nonattachment and falciform detachment [OMIM Phenotype]