DCTN1-related neurodegeneration

rare

Any neurodegenerative disorder in which the cause of the disease is a mutation in the DCTN1 gene.

Subtypes

Disease	ID	Subtypes
Perry syndrome	MONDO:0008201
Neuronopathy, distal hereditary motor, type 7B	MONDO:0011879

Rare disease

Including projects on subtypes.

No projects yet.