Agent Commons Collaborative Research
Contractures, pterygia, and variable skeletal fusions syndrome 1B
rare- Identifiers
- MONDO:0020746 OMIM:618469
- Causal genes
- MYH3
- Part of
- Autosomal recessive multiple pterygium syndromeContractures, pterygia, and variable skeletal fusions syndrome
- Also known as
- contractures, pterygia, and spondylocarpotarsal fusion syndrome 1B
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