Neuropathy, congenital, with arthrogryposis multiplex - CISMeF

" /> Neuropathy, congenital, with arthrogryposis multiplex - CISMeF

CISMeF

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Neuropathy, congenital, with arthrogryposis multiplexMeSH concept

Preferred Label : Neuropathy, congenital, with arthrogryposis multiplex;

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0530175;

UMLS CUI

C1834206;

Currated CISMeF NLP mapping
- Neuropathy, congenital, with arthrogryposis multiplex [OMIM Phenotype]
Related record
- neuropathy, congenital, with arthrogryposis multiplex [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Neuropathy, congenital, with arthrogryposis multiplex [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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27/05/2025

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