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

1 clinical trial for this condition and its sub-types, 0 tagged with Digitotalar dysmorphism itself.

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Where it sits in the disease tree

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↑ Multiple congenital anomalies/dysmorphic syndrome without intellectual disability (163) ↑ Distal arthrogryposis (3)

Sub-types of Digitotalar dysmorphism

Arthrogryposis, distal, type 1A 0 trials
Arthrogryposis, distal, type 1B 0 trials
Digitotalar dysmorphism; ulnar drift, hereditary 0 trials

Including sub-types (1) Tagged with Digitotalar dysmorphism (0)

Completed 1

Kids test new bionic foot design

Knowledge-focused Completed

This study tested a new prosthetic foot for children with leg amputations or birth defects. Thirteen kids walked with the device and gave feedback on stiffness and performance. The goal was to gather ideas to improve future foot designs.

Sponsor: Össur Iceland ehf • Aim: Knowledge-focused

Last updated Jun 27, 2026 14:00 UTC

Digitotalar dysmorphism

Where it sits in the disease tree

Kids test new bionic foot design