RS864321670 ALDH18A1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary spastic paraplegia 9A
ALDH18A1 deficiency
de Barsy syndrome
Cutis laxa
autosomal dominant 3
Autosomal dominant spastic paraplegia type 9
Hereditary spastic paraplegia 9A
ALDH18A1 deficiency
de Barsy syndrome
Cutis laxa
autosomal dominant 3
Autosomal dominant spastic paraplegia type 9
Other Variants in ALDH18A1