(Q4420136)
(Redirected from Q56014299)
English
multicentric osteolysis-nodulosis-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.
- Torg-Winchester Syndrome
- MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY
- Osteolysis, Hereditary Multicentric
- MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA
- MONA
- Nao Syndrome
- Torg-Winchester Syndrome, Formerly
- Torg Syndrome
- Nodulosis-Arthropathy-Osteolysis Syndrome
- Al-Aqeel Sewairi Syndrome
- Nodulosis–arthropathy–osteolysis syndrome
- Hereditary multicentric osteolysis
- Multicentric osteolysis, nodulosis and arthropathy
- Nodulosis-arthropathy-osteolysis syndrome
- Multicentric osteolysis-nodulosis-arthropathy syndrome
- NAO syndrome
Statements
C123437
1 reference
Identifiers
1 reference
1 reference
1 reference
2 references
Sitelinks
Wikipedia(2 entries)
- dewiki MONA-Spektrum
- enwiki Nodulosis–arthropathy–osteolysis syndrome