Digitotalar dysmorphism

MONDO:0015240

Digitotalar dysmorphism, also known as distal arthrogryposis type 1 (DA1), is an autosomal dominant congenital anomaly characterized by contractures of the distal regions of the hands and feet with no facial involvement or any additional anomalies. It is the most common type of distal arthrogryposis.

Also known as: DA1, arthrogryposis multiplex congenita distal type 1, digitotalar dysmorphism, distal arthrogryposis type 1, distal arthrogryposis type 1A (sub-type), distal arthrogryposis type 1B (sub-type), AMCD1

38 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Sub-types

Broader categories

Sort by