multicentric osteolysis-nodulosis-arthropathy (Q4420136)

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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
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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

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