neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive

Preferred Label : neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive;

MeSH note : mutation in CCT5;

Origin ID

C564948;

UMLS CUI

C1850395;

Currated CISMeF NLP mapping
- Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive [OMIM Phenotype]
MeSH term(s) associated for indexing
- hereditary sensory and motor neuropathy [MeSH Descriptor]
Record concept(s)
- neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Mutilating hereditary sensory neuropathy with spastic paraplegia [ORDO Disease]
- Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive [OMIM Phenotype]