nakamura osame syndrome

Preferred Label : nakamura osame syndrome;

MeSH synonym : spastic paraplegia, mental retardation and thin corpus callosum;

Origin ID

C538335;

UMLS CUI

C2931821;

Currated CISMeF NLP mapping
- Autosomal recessive spastic paraplegia type 11 [ICD-11 More detail]
- Autosomal recessive spastic paraplegia type 11 [ORDO Disease]
- Autosomal recessive spastic paraplegia type 11 (disorder) [SNOMED CT concept]
- Spastic Paraplegia 11 [NCIt concept]
- Spastic paraplegia 11, autosomal recessive [OMIM Phenotype]
- hereditary spastic paraplegia 11 [DO Concept]
MeSH term(s) associated for indexing
- agenesis of corpus callosum [MeSH Descriptor]
- intellectual disability [MeSH Descriptor]
- spastic paraplegia, hereditary [MeSH Descriptor]
ORDO relation(s)
- Autosomal recessive spastic paraplegia type 11 [ORDO Disease]
Record concept(s)
- Nakamura Osame syndrome [MeSH concept]
See also inter- (CISMeF)
- Autosomal recessive spastic paraplegia type 11 [ICD-11 More detail]
- Autosomal recessive spastic paraplegia type 11 [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive spastic paraplegia type 11 (disorder) [SNOMED CT concept]