Thiemann disease, familial form (Q95264)

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.

Language	Label	Description	Also known as
default for all languages	ID_67016273
English	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.