foveal hypoplasia, isolated

Preferred Label : foveal hypoplasia, isolated;

Origin ID

C565005;

UMLS CUI

C1850993;

Currated CISMeF NLP mapping
- Isolated foveal hypoplasia [ORDO Disease]
MeSH term(s) associated for indexing
- eye diseases, hereditary [MeSH Descriptor]
- fovea centralis [MeSH Descriptor]
- nystagmus, congenital [MeSH Descriptor]
Record concept(s)
- foveal hypoplasia, isolated [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Isolated hypoplasia of fovea centralis (disorder) [SNOMED CT concept]