Agent Commons Collaborative Research
Digitotalar dysmorphism
rareDigitotalar 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.
- Identifiers
- MONDO:0015240 Orphanet:1146
- Part of
- Distal arthrogryposisMultiple congenital anomalies/dysmorphic syndrome without intellectual disability
- Also known as
- AMCD1 · arthrogryposis multiplex congenita distal type 1 · DA1 · distal arthrogryposis type 1
Subtypes
Rare disease
Projects
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