neuropathy, congenital, with arthrogryposis multiplex

Preferred Label : neuropathy, congenital, with arthrogryposis multiplex;

MeSH synonym : congenital non-progressive peripheral neuropathy with arthrogryposis multiplex;

Details

Origin ID

C535714;

UMLS CUI

C1834206;

Currated CISMeF NLP mapping
- Neuropathy, congenital, with arthrogryposis multiplex [OMIM Phenotype]
MeSH term(s) associated for indexing
- arthrogryposis [MeSH Descriptor]
Record concept(s)
- Neuropathy, congenital, with arthrogryposis multiplex [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Neuropathy, congenital, with arthrogryposis multiplex [OMIM Phenotype]

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