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MIM:607641 - NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB; HMN7B
Xenbase Genes: dctn1
Human Disease Resource: MIM
MONDO:0011879 - neuronopathy, distal hereditary motor, type 7B |
MONDO:0015355 - distal hereditary motor neuropathy type 7 |
Disease Ontology (DO):
DOID:0111202 - autosomal dominant distal hereditary motor neuronopathy 14 |