Digitotalar dysmorphism
MONDO:0015240Digitotalar 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.
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Broader categories
Disease
(618)
Musculoskeletal system disorder
(196)
Hereditary disease
(172)
Muscle tissue disorder
(53)
Human disease
(14)
Developmental defect during embryogenesis
(7)
Congenital limb malformation
(3)
Disease of genetic or genomic mechanism
(2)
Multiple congenital anomalies/dysmorphic syndrome
(1)
Arthrogryposis syndrome
(0)