has material basis in germline mutation in MMP2 syndromic disease multicentric osteolysis, nodulosis, and arthropathy https://github.com/monarch-initiative/mondo/issues/4948 https://github.com/monarch-initiative/mondo/issues/5784 https://www.malacards.org/card/multicentric_osteolysis_nodulosis_and_arthropathy GARD:0013743 Torg syndrome Torg-Winchester syndrome NAO syndrome nodulosis-arthropathy-osteolysis syndrome MONA, MMP2-related multicentric osteolysis, nodulosis, and arthropathy A rare, autosomal recessive inherited syndrome caused by mutations in the MMP2 gene. It is characterized by the presence of multiple, painless subcutaneous nodules, osteolysis particularly in the hands and feet, osteoporosis, and arthropathy. Winchester-Torg syndrome MONA OMIM:259600 multicentric osteolysis, nodulosis and arthropathy, MMP2-related osteolysis, hereditary multicentric NCIT:C123437 Al-Aqeel Sewairi syndrome MONDO:0009809 multicentric osteolysis-nodulosis-arthropathy spectrum