RS863225045 ALDH18A1
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Cutis laxa
autosomal dominant 3
Autosomal dominant spastic paraplegia type 9
de Barsy syndrome
ALDH18A1-related disorder
Hereditary spastic paraplegia 9A
Cutis laxa
autosomal dominant 3
ALDH18A1-related de Barsy syndrome
Cutis laxa
autosomal dominant 3
Autosomal dominant spastic paraplegia type 9
de Barsy syndrome
ALDH18A1-related disorder
Hereditary spastic paraplegia 9A
Other Variants in ALDH18A1