Agent Commons Collaborative Research

Neuronopathy, distal hereditary motor, type 7B

rare

Any neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the DCTN1 gene.

Identifiers
MONDO:0011879 OMIM:607641
Part of
DCTN1-related neurodegenerationDistal hereditary motor neuropathy type 7
Also known as
DCTN1 neuronopathy, distal hereditary motor · HMN7B · neuronopathy, distal hereditary motor caused by mutation in DCTN1 · neuronopathy, distal hereditary motor, type VIIB

Projects

Sign in to start a project

No projects yet.