Charcot-Marie-Tooth disease, axonal, type 2a1

Preferred Label : Charcot-Marie-Tooth disease, axonal, type 2a1;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0566438;

UMLS CUI

C1861678;

Currated CISMeF NLP mapping
- Autosomal dominant Charcot-Marie-Tooth disease type 2A1 [ORDO Disease]
- Autosomal dominant Charcot-Marie-Tooth disease type 2A1 (disorder) [SNOMED CT concept]
- Charcot-Marie-Tooth Disease Type 2A1 [NCIt concept]
- Charcot-Marie-Tooth disease type 2A1 [DO Concept]
- Charcot-Marie-Tooth disease type 2A1 [ICD-11 More detail]
- Charcot-marie-tooth disease, axonal, type 2a1 [OMIM Phenotype]
Related record
- Charcot-Marie-Tooth disease, axonal, type 2a1 [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant Charcot-Marie-Tooth disease type 2A1 [ORDO Disease]
- Autosomal dominant Charcot-Marie-Tooth disease type 2A1 (disorder) [SNOMED CT concept]
- Charcot-Marie-Tooth Disease Type 2A1 [NCIt concept]
- Charcot-marie-tooth disease, axonal, type 2a1 [OMIM Phenotype]