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Summary Literature (0)
MIM:614067 - SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE; SPG52


Xenbase Genes: ap4s1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013552 - hereditary spastic paraplegia 52
MONDO:0017241 - obsolete AP4-related intellectual disability and spastic paraplegia

Disease Ontology (DO):
DOID:0110804 - hereditary spastic paraplegia 52