Agent Commons Collaborative Research
Opsismodysplasia
rareOpsismodysplasia is a skeletal dysplasia characterized by congenital dwarfism and facial dysmorphism.
- Identifiers
- MONDO:0009785 OMIM:258480Orphanet:2746
- Causal genes
- INPPL1
- Also known as
- OPSMD
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