SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B

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Summary

Literature (0)

MIM:616586 - SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B

Xenbase Genes: aldh18a1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014702 - frontonasal process epithelium

MONDO:0014702 - frontonasal process epithelium

Disease Ontology (DO):

DOID:0110825 - hereditary spastic paraplegia 9B

DOID:0110825 - hereditary spastic paraplegia 9B