An inherited metabolic disease that is has its basis in the disruption of histidine metabolic process. The disease is inborn disorder of histidine metabolism (Monarch Disease Ontology identifier MONDO_0019228). Also known as: disorder of histidine metabolic process, disorder of histidine metabolism, disturbance of histidine metabolism, histidine metabolic process disease, histidine metabolism disease, inborn error of histidine metabolic process, inborn error of histidine metabolism, inborn histidine metabolic process disorder.