optic atrophy spastic paraplegia syndrome

Preferred Label : optic atrophy spastic paraplegia syndrome;

Origin ID

C564084;

UMLS CUI

C1839565;

Automatic exact mappings (from CISMeF team)
- Optic atrophy--spastic paraplegia syndrome [OMIM Phenotype]
MeSH term(s) associated for indexing
- optic atrophies, hereditary [MeSH Descriptor]
- paraplegia [MeSH Descriptor]
Record concept(s)
- optic atrophy spastic paraplegia syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Optic atrophy--spastic paraplegia syndrome [OMIM Phenotype]