Idiopathic Basal Ganglia Calcification 1

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal dominant condition caused by mutation(s) in the SLC20A2 gene, encoding sodium-dependent phosphate transporter 2. It is characterized by calcification of the basal ganglia.

**Synonyms:** - BSPDC - Bilateral Striopallidodentate Calcinosis - IBGC1