neuropathy, hereditary sensorimotor, with upper motor neuron, visual pathway and autonomic disturbance

Preferred Label : neuropathy, hereditary sensorimotor, with upper motor neuron, visual pathway and autonomic disturbance;

Origin ID

C563517;

UMLS CUI

C1834205;

Automatic exact mappings (from CISMeF team)
- Neuropathy, hereditary sensorimotor, with upper motor neuron, visual pathway and autonomic disturbance [OMIM Phenotype]
MeSH term(s) associated for indexing
- dysautonomia, familial [MeSH Descriptor]
- eye diseases [MeSH Descriptor]
- hereditary sensory and motor neuropathy [MeSH Descriptor]
- motor neuron disease [MeSH Descriptor]
Record concept(s)
- neuropathy, hereditary sensorimotor, with upper motor neuron, visual pathway and autonomic disturbance [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Neuropathy, hereditary sensorimotor, with upper motor neuron, visual pathway and autonomic disturbance [OMIM Phenotype]