SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE; SPG78

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Summary

Literature (0)

MIM:617225 - SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE; SPG78

Xenbase Genes: atp13a2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014975 - autosomal recessive spastic paraplegia type 78

MONDO:0014975 - autosomal recessive spastic paraplegia type 78

Disease Ontology (DO):

DOID:0112348 - hereditary spastic paraplegia 78

DOID:0112348 - hereditary spastic paraplegia 78