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digitotalar dysmorphism

Disease Summary
Associated Targets (6)
Tbio

5

Tchem

1


GARD Rare
Mondo Description 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.
Mondo Term and Equivalent IDs
MONDO:0015240:  digitotalar dysmorphism
GARD:0000787: 
Orphanet:1146: 
UMLS:C0220662: 
UMLS:C1852085: 
UMLS:CN197602: