SPASTIC PARAPLEGIA 82, AUTOSOMAL RECESSIVE; SPG82

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:618770 - SPASTIC PARAPLEGIA 82, AUTOSOMAL RECESSIVE; SPG82

Xenbase Genes:

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0032906 - spastic paraplegia 82, autosomal recessive

MONDO:0032906 - spastic paraplegia 82, autosomal recessive

Disease Ontology (DO):

DOID:0112343 - hereditary spastic paraplegia 82

DOID:0112343 - hereditary spastic paraplegia 82