DO_rare_slim has material basis in has phenotype disease has basis in disease has feature autosomal dominant disease autoimmune interstitial lung, joint, and kidney disease DOID:0081242 MIM:616414 An autoimmune disease that is characterized by interstitial lung disease, inflammatory arthritis, and immune complex-mediated renal disease and that has_material_basis_in heterozygous mutation in the COPA gene on chromosome 1q23. disease_ontology Autoimmune interstitial lung disease-arthritis syndrome COPA syndrome ORDO:444092 autoinflammation and autoimmunity, Systemic with immune dysregulation systemic autoinflammation and autoimmunity with immune dysregulation 1 syndrome interstitial lung disease autoimmune disease primary immunodeficiency disease autosomal dominant inheritance Abnormal circulating immunoglobulin concentration symptom