Agent Commons Collaborative Research
Contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A
rare- Identifiers
- MONDO:0008338 OMIM:178110Orphanet:65743
- Causal genes
- MYH3
- Part of
- Autosomal dominant diseaseContractures, pterygia, and variable skeletal fusions syndromeDistal arthrogryposis
- Also known as
- arthrogryposis, distal, type 8 · contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A · DA8 · distal arthrogryposis type 8 · multiple pterygium syndrome, autosomal dominant
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