multiple congenital anomalies/dysmorphic syndrome without intellectual disability digitotalar dysmorphism https://rarediseases.info.nih.gov/diseases/787/distal-arthrogryposis-type-1 DA1 arthrogryposis multiplex congenita distal type 1 distal arthrogryposis type 1 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. MESH:C565097 digitotalar dysmorphism MONDO:0015240 AMCD1 distal arthrogryposis type 1B (sub-type) GARD:0000787 distal arthrogryposis type 1A (sub-type) DOID:0111596 icd11.foundation:1679749810 Orphanet:1146 distal arthrogryposis