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ACTC1-related distal arthrogryposis with congenital heart disease

MONDO:0700352

A distal arthrogryposis caused by variation in the ACTC1 gene. This disease is characterised by multiple congenital contractures, neck pterygia, scoliosis, congenital heart defects, and/or cardiomyopathy.

76 clinical trials for this condition and its sub-types, 0 tagged with ACTC1-related distal arthrogryposis with congenital heart disease itself.

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Part of

↑ Cardiogenetic disease (618) ↑ Congenital heart disease (419) ↑ Distal arthrogryposis (3)
Including sub-types (76) Tagged with ACTC1-related distal arthrogryposis with congenital heart disease (0)
Trials to join now! 34 Not yet recruiting 12 Not yet finished but already full! 11 Completed 18 Terminated 1
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