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Disease association ontology term - MONDO:0100624 - DCTN1-related neurodegeneration

Term summary

ID
MONDO:0100624
Name
DCTN1-related neurodegeneration
Ontology or CV name
Disease association
Definition
Any neurodegenerative disorder 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:

MONDO:0008201 - Perry syndrome

References:

Genes: