Preferred Label : Parkinson Disease 9;
NCIt synonyms : KRS; PARK9; Kufor-Rakeb Syndrome;
NCIt definition : An autosomal recessive subtype of Parkinson disease, caused by mutation(s) in the
ATP13A2 gene, encoding polyamine-transporting ATPase 13A2.;
Origin ID : C203534;
- Has associated anatomic sites
- concept_is_in_subset