has material basis in germline mutation in MVK immune system disorder hyperimmunoglobulinemia D with periodic fever https://github.com/monarch-initiative/mondo/issues/6747 https://www.malacards.org/card/hyper_igd_syndrome OMIM:260920 NANDO:1200866 Orphanet:343 NANDO:2200436 GARD:0002788 DOID:0081450 MONDO:0009849 MEDGEN:140768 hyperimmunoglobulinemia D syndrome periodic fever Dutch type UMLS:C0398691 partial mevalonate kinase deficiency HIDS hyper-IgD syndrome Hyperimmunoglobinemia D with periodic fever (HIDS) is a rare autoinflammatory disease characterized by periodic attacks of fever and a systemic inflammatory reaction (cervical lymphadenopathy, abdominal pain, vomiting, diarrhea, arthralgias and skin signs). hyperimmunoglobinemia D with recurrent fever hyper IgD syndrome mevalonate kinase deficiency