|
MIM:616586 - SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B
Xenbase Genes: aldh18a1
Human Disease Resource: MIM
MONDO:0014702 - autosomal recessive complex spastic paraplegia type 9B |
DOID:0110825 - hereditary spastic paraplegia 9B |
|
MONDO:0014702 - autosomal recessive complex spastic paraplegia type 9B |
DOID:0110825 - hereditary spastic paraplegia 9B |