Neuropathy, painful

Preferred Label : Neuropathy, painful;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive;

Prefixed ID : 256870;

Details

Origin ID

256870;

UMLS CUI

C1850383;

Automatic exact mappings (from CISMeF team)
- neuralgia [MeSH Descriptor]
Currated CISMeF NLP mapping
- neuropathy, painful [MeSH concept]
- neuropathy, painful [MeSH Supplementary Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Fever [HPO term]
- Infantile onset [HPO term]
- Lower limb muscle weakness [HPO term]
- Peripheral neuropathy [HPO term]
- Skeletal muscle atrophy [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- neuropathy, painful [MeSH Supplementary Concept]
- neuropathy, painful [MeSH concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients