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Summary Literature (0)
MIM:614066 - SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47

Xenbase Genes: ap4b1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013551 - hereditary spastic paraplegia 47
MONDO:0017241 - obsolete AP4-related intellectual disability and spastic paraplegia

Disease Ontology (DO):
DOID:0110799 - hereditary spastic paraplegia 47