Neuropathy, with paraprotein in serum, cerebrospinal fluid and urine

Preferred Label : Neuropathy, with paraprotein in serum, cerebrospinal fluid and urine;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 162600;

Details

Origin ID

162600;

UMLS CUI

C1834180;

Currated CISMeF NLP mapping
- neuropathy, with paraprotein in serum, cerebrospinal fluid and urine [MeSH concept]
- neuropathy, with paraprotein in serum, cerebrospinal fluid and urine [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Decreased nerve conduction velocity [HPO term]
- Demyelination [HPO term]
- Peripheral demyelination [HPO term]
- Peripheral neuropathy [HPO term]
- Polyneuritis [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- neuropathy, with paraprotein in serum, cerebrospinal fluid and urine [MeSH Supplementary Concept]
- neuropathy, with paraprotein in serum, cerebrospinal fluid and urine [MeSH concept]

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