Disease association ontology term - MONDO:0011002 - neuropathy, hereditary motor and sensory, type 6A

Term summary

ID

MONDO:0011002

Name

neuropathy, hereditary motor and sensory, type 6A

Ontology or CV name

Disease association

Definition

Any hereditary motor and sensory neuropathy type 6 in which the cause of the disease is a mutation in the MFN2 gene.

Parents

• is_a motor peripheral neuropathy
• is_a Charcot-Marie-Tooth disease
• is_a hereditary motor and sensory neuropathy type 6

Annotation