Disease association ontology term - MONDO:0014711 - autosomal dominant Charcot-Marie-Tooth disease type 2W
Term summary
- ID
- MONDO:0014711
- Name
- autosomal dominant Charcot-Marie-Tooth disease type 2W
- Ontology or CV name
- Disease association
- Definition
- Any Charcot-Marie-Tooth disease type 2 in which the cause of the disease is a mutation in the HARS gene.