RS137852696 PPT1
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What This Variant Does
"Neuronal ceroid lipofuscinosis (PPT1-related) [OMIM:?]
Associated Conditions
Neuronal ceroid lipofuscinosis 1
Retinitis pigmentosa
Inborn genetic diseases
PPT1-related disorder
Neuronal ceroid lipofuscinosis 1
Retinitis pigmentosa
Inborn genetic diseases
PPT1-related disorder
Other Variants in PPT1