Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:616907 - SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE; SPG76

Xenbase Genes: capn1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014827 - autosomal recessive spastic paraplegia type 76