Charcot-Marie-Tooth disease, type 2I

Preferred Label : Charcot-Marie-Tooth disease, type 2I;

MeSH synonym : Charcot-Marie-Tooth disease, axonal, type 2I; CMT 2I; Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2l; CMT2I; Charcot-Marie-Tooth neuropathy, axonal, type 2l; Cmt2l;

Details

Origin ID

C535416;

UMLS CUI

C3888087;

Currated CISMeF NLP mapping
- Autosomal dominant Charcot-Marie-Tooth disease type 2I [ORDO Disease]
- Autosomal dominant Charcot-Marie-Tooth disease type 2I (disorder) [SNOMED CT concept]
- Autosomal dominant Charcot-Marie-Tooth disease type 2L [ORDO Disease]
- Autosomal dominant Charcot-Marie-Tooth disease type 2L (disorder) [SNOMED CT concept]
- Charcot-Marie-Tooth disease axonal type 2L [DO Concept]
- Charcot-Marie-Tooth disease type 2I [DO Concept]
- Charcot-marie-tooth disease, axonal, type 2i [OMIM Phenotype]
- Charcot-marie-tooth disease, axonal, type 2l [OMIM Phenotype]
MeSH term(s) associated for indexing
- charcot-marie-tooth disease [MeSH Descriptor]
Record concept(s)
- Charcot-Marie-Tooth disease, Type 2I [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant Charcot-Marie-Tooth disease type 2I [ORDO Disease]
- Autosomal dominant Charcot-Marie-Tooth disease type 2I (disorder) [SNOMED CT concept]
- Autosomal dominant Charcot-Marie-Tooth disease type 2L [ORDO Disease]
- Charcot-marie-tooth disease, axonal, type 2i [OMIM Phenotype]

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