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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.

Parents

Annotation

Disease association

MONDO:0014711 - autosomal dominant Charcot-Marie-Tooth disease type 2W

References:

Genes: