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congenital radioulnar synostosis

Disease Summary
Associated Targets ()

Mondo Description Congenital radioulnar synostosis is a rare bone disorder that may be isolated or associated with other disorders and that is characterized by failure of segmentation of the radius and ulna during embryological development, causing limited rotational movements of the forearm, which may lead to difficulties with some activities of daily living.
Mondo Term and Equivalent IDs
MONDO:0017985:  congenital radioulnar synostosis
COHD:438851: 
GARD:0004630: 
GARD:0010876: 
ICD9:755.53: 
MESH:C562408: 
Orphanet:3269: 
SCTID:33313004: