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Disease association ontology term - MONDO:0011879 - neuronopathy, distal hereditary motor, type 7B

Term summary

ID
MONDO:0011879
Name
neuronopathy, distal hereditary motor, type 7B
Ontology or CV name
Disease association
Definition
Any neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the DCTN1 gene.

Parents

Annotation

Disease association

MONDO:0011879 - neuronopathy, distal hereditary motor, type 7B

References:

Genes: