Charcot-Marie-Tooth disease, type 4A, axonal form

Preferred Label : Charcot-Marie-Tooth disease, type 4A, axonal form;

MeSH synonym : CMT2 with vocal cord paresis, autosomal recessive; Charcot-Marie-Tooth neuropathy, axonal, with vocal cord paresis, autosomal recessive; Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive;

Related MeSH term : CMT 2G; Cmt2g; Charcot-Marie-Tooth disease, axonal, Type 2G; Charcot-Marie-Tooth Neuropathy, Type 2g;

Détails

Origin ID

C539595;

UMLS CUI

C1843183;

Automatic exact mappings (from CISMeF team)
- Autosomal dominant Charcot-Marie-Tooth disease type 2G [ORDO Disease]
- Charcot-marie-tooth disease, axonal, type 2p [OMIM Phenotype]
Currated CISMeF NLP mapping
- Charcot-Marie-Tooth disease type 2G [ICD-11 More detail]
MeSH term(s) associated for indexing
- charcot-marie-tooth disease [MeSH Descriptor]
Record concept(s)
- Charcot-Marie-Tooth disease, Type 2G [MeSH concept]
- Charcot-Marie-Tooth disease, Type 4A, axonal form [MeSH concept]
See also inter- (CISMeF)
- Charcot-marie-tooth disease, axonal, with vocal cord paresis, autosomal recessive [OMIM Phenotype]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Charcot-marie-tooth disease, axonal, with vocal cord paresis, autosomal recessive [OMIM Phenotype]

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