RS369465821 PNPLA6
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Associated Conditions
Hereditary spastic paraplegia 39
Inborn genetic diseases
Trichomegaly-retina pigmentary degeneration-dwarfism syndrome
Laurence-Moon syndrome
Hereditary spastic paraplegia 39
Inborn genetic diseases
Trichomegaly-retina pigmentary degeneration-dwarfism syndrome
Laurence-Moon syndrome
Other Variants in PNPLA6