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;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Hmsn with excessive myelin outfolding, autosomal recessive; Charcot-marie-tooth disease with excessive myelin folding, autosomal recessive;

Prefixed ID : %256855;

Details

Origin ID

256855;

UMLS CUI

C1850385;

Currated CISMeF NLP mapping
- neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive [MeSH concept]
- neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive [MeSH Supplementary 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 [MeSH Supplementary Concept]
- neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive [MeSH concept]

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