SPASTIC PARAPLEGIA 72A, AUTOSOMAL DOMINANT; SPG72A

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Summary

Literature (0)

MIM:615625 - SPASTIC PARAPLEGIA 72A, AUTOSOMAL DOMINANT; SPG72A

Xenbase Genes: reep2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014282 - hereditary spastic paraplegia 72

MONDO:0014282 - hereditary spastic paraplegia 72

Disease Ontology (DO):

DOID:0110817 - hereditary spastic paraplegia 72A

DOID:0110817 - hereditary spastic paraplegia 72A