This can be seen in Figure 6, which shows superimposed results (GPT-3.5 only) for genes associated with the Human Phenotype Ontology term “Sensory ataxia” (HP:0010871; EGR2 NAGLU GPI DNAJC3 SH3TC2 TWNK PIEZO2 FLVCR1 MPZ PRX PMP22 KPNA3 POLG RNF170 AARS1). The gene discussed is RNF170; the disease is sensory ataxia.