Thiemann disease, familial form (Q95264)

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Thiemann disease is a very rare genetic necrotic bone disorder characterised clinically by painless swelling of the proximal interphalangeal joints associated with osteonecrosis of epiphyses followed by osteoarthritic changes, with onset before 25 years of age and often a benign course.
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    Thiemann disease, familial form
    Thiemann disease is a very rare genetic necrotic bone disorder characterised clinically by painless swelling of the proximal interphalangeal joints associated with osteonecrosis of epiphyses followed by osteoarthritic changes, with onset before 25 years of age and often a benign course.

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