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OMIM:605280 - SPASTIC PARAPLEGIA 13, AUTOSOMAL DOMINANT; SPG13
DOID:0110766 - hereditary spastic paraplegia 13 |
MONDO:0011532 - hereditary spastic paraplegia 13 |
Human Disease Resources: OMIM
Xenbase Genes: hspd1
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DOID:0110766 - hereditary spastic paraplegia 13 |
MONDO:0011532 - hereditary spastic paraplegia 13 |