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Disease association ontology term - MONDO:0013644 - Charcot-Marie-Tooth disease axonal type 2O

Term summary

ID
MONDO:0013644
Name
Charcot-Marie-Tooth disease axonal type 2O
Ontology or CV name
Disease association
Definition
Any Charcot-Marie-Tooth disease in which the cause of the disease is a mutation in the DYNC1H1 gene.

Parents

Annotation

Disease association

MONDO:0013644 - Charcot-Marie-Tooth disease axonal type 2O

References:

Genes: