Multicentric osteolysis, nodulosis, and arthropathy

MONDO:0009809

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.

Also known as: Al-Aqeel Sewairi syndrome, MONA, MONA, MMP2-related, NAO syndrome, Torg syndrome, Winchester-Torg syndrome, multicentric osteolysis, nodulosis and arthropathy, MMP2-related, multicentric osteolysis, nodulosis, and arthropathy

35 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by