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 (1)
MIM:600363 - SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT; SPG6

Xenbase Genes: nipa1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010878 - hereditary spastic paraplegia 6

Disease Ontology (DO):
DOID:0110811 - hereditary spastic paraplegia 6