Autosomal dominant Charcot-Marie-Tooth disease type 2N - CISMeF

" /> Autosomal dominant Charcot-Marie-Tooth disease type 2N - CISMeF

CISMeF

chu

Autosomal dominant Charcot-Marie-Tooth disease type 2NICD-11 More detail

Preferred Label : Autosomal dominant Charcot-Marie-Tooth disease type 2N;

Details

Origin ID

821001900;

Currated CISMeF NLP mapping
- Autosomal dominant Charcot-Marie-Tooth disease type 2N [ORDO Disease]
- Autosomal dominant Charcot-Marie-Tooth disease type 2N (disorder) [SNOMED CT concept]
- Charcot-Marie-Tooth disease axonal type 2N [DO Concept]
- Charcot-Marie-Tooth disease, axonal, type 2n [MeSH concept]
- Charcot-Marie-Tooth disease, axonal, type 2n [MeSH Supplementary Concept]
- Charcot-marie-tooth disease, axonal, type 2n [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients

Nous contacter.
17/06/2024

© Rouen University Hospital. Any partial or total use of this material must mention the source.