Disease association ontology term - MONDO:0014975 - autosomal recessive spastic paraplegia type 78

Term summary

ID

MONDO:0014975

Name

autosomal recessive spastic paraplegia type 78

Ontology or CV name

Disease association

Definition

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the ATP13A2 gene.

Parents

• is_a autosomal recessive disease
• is_a complex hereditary spastic paraplegia

Annotation