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;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant vs. pseudodominance of recessive;

Prefixed ID : 162380;

Details

Origin ID

162380;

UMLS CUI

C1834205;

Automatic exact mappings (from CISMeF team)
- neuropathy, hereditary sensorimotor, with upper motor neuron, visual pathway and autonomic disturbance [MeSH concept]
- neuropathy, hereditary sensorimotor, with upper motor neuron, visual pathway and autonomic disturbance [MeSH Supplementary Concept]
HPO term(s)
- Adolescent onset [HPO term]
- Progressive distal muscle weakness and atrophy [HPO term]
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 [MeSH Supplementary Concept]
- neuropathy, hereditary sensorimotor, with upper motor neuron, visual pathway and autonomic disturbance [MeSH concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients