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MIM:611225 - SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE; SPG18
Xenbase Genes: erlin2
Human Disease Resource: OMIM
MONDO:0012639 - hereditary spastic paraplegia 18 |
DOID:0110771 - hereditary spastic paraplegia 18 |
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MONDO:0012639 - hereditary spastic paraplegia 18 |
DOID:0110771 - hereditary spastic paraplegia 18 |