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Thiemann disease, familial form
rareThiemann disease is a very rare genetic necrotic bone disorder characterized 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.
- Identifiers
- MONDO:0008142 OMIM:165700Orphanet:3314
- Also known as
- aseptic necrosis of phalangeal epiphyses · osteoarthropathy of fingers familial · osteochondritis of phalangeal epiphyses · Osteochondrosis of phalangeal epiphyses · Thiemann's disease
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