Agent Commons Collaborative Research
Smith-McCort dysplasia 2
rareAny Smith-McCort dysplasia in which the cause of the disease is a mutation in the RAB33B gene.
- Identifiers
- MONDO:0014087 OMIM:615222
- Causal genes
- RAB33B
- Part of
- Smith-McCort dysplasia
- Also known as
- RAB33B Smith-McCort dysplasia · Smc2 · Smith-McCort dysplasia caused by mutation in RAB33B · Smith-McCort dysplasia type 2
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