neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive

Preferred Label : neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive;

MeSH synonym : Charcot-Marie-Tooth disease with excessive myelin folding, autosomal recessive;

Details

Origin ID

C564947;

UMLS CUI

C1850385;

Currated CISMeF NLP mapping
- Neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive [OMIM Phenotype]
MeSH term(s) associated for indexing
- hereditary sensory and motor neuropathy [MeSH Descriptor]
Record concept(s)
- neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive [OMIM Phenotype]

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