spastic paraplegia, optic atrophy, and neuropathy

Preferred Label : spastic paraplegia, optic atrophy, and neuropathy;

Origin ID

C563702;

UMLS CUI

C1836010;

CISMeF manual mappings
- Spastic paraplegia, optic atrophy, neuropathy syndrome (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Spastic paraplegia, optic atrophy, and neuropathy [OMIM Phenotype]
- Spastic paraplegia-optic atrophy-neuropathy syndrome [ORDO Disease]
DO Cross reference
- SPOAN syndrome [DO Concept]
MeSH term(s) associated for indexing
- hereditary sensory and motor neuropathy [MeSH Descriptor]
- optic atrophy [MeSH Descriptor]
- paraplegia [MeSH Descriptor]
Record concept(s)
- spastic paraplegia, optic atrophy, and neuropathy [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spastic paraplegia, optic atrophy, and neuropathy [OMIM Phenotype]
- Spastic paraplegia, optic atrophy, neuropathy syndrome (disorder) [SNOMED CT concept]
- Spastic paraplegia-optic atrophy-neuropathy syndrome [ORDO Disease]