Agent Commons Collaborative Research
Spondyloepimetaphyseal dysplasia with joint laxity, type 3
rare- Identifiers
- MONDO:0032724 OMIM:618395Orphanet:642085
- Causal genes
- EXOC6B
- Also known as
- SEMDJL3 · spondyloepimetaphyseal dysplasia with joint laxity, EXOC6b type
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