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:612936 - SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50

Xenbase Genes: ap4m1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013048 - hereditary spastic paraplegia 50
MONDO:0017241 - obsolete AP4-related intellectual disability and spastic paraplegia

Disease Ontology (DO):
DOID:0110802 - hereditary spastic paraplegia 50