has material basis in germline mutation in VAC14 striatonigral degeneration striatonigral degeneration, childhood-onset https://www.malacards.org/card/striatonigral_degeneration_childhood_onset OMIM:617054 Lenk-Ploski syndrome GARD:0017918 SNDC Orphanet:497906 UMLS:C4310743 MEDGEN:934710 childhood-onset basal ganglia degeneration syndrome striatonigral degeneration, childhood-onset; SNDC MONDO:0014889 striatonigral Degeneration, childhood-onset inherited dystonia