In particular, several Sst subtypes, Vip_Cbln1 and Id2_Lamp5 subtypes showed high enrichment for DO terms such as focal epilepsy (DOID:2234), epilepsy syndrome (DOID:1826), and temporal lobe epilepsy (DOID:3328) (Source Data Table 12). The gene discussed is CBLN1; the disease is epilepsy syndrome.