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Disease association ontology term - MONDO:0013634 - neuropathy, hereditary sensory, type 2C

Term summary

ID
MONDO:0013634
Name
neuropathy, hereditary sensory, type 2C
Ontology or CV name
Disease association
Definition
Any hereditary sensory and autonomic neuropathy type 2 in which the cause of the disease is a mutation in the KIF1A gene.

Parents

Annotation

Disease association

MONDO:0013634 - neuropathy, hereditary sensory, type 2C

References:

Genes: