Agent Commons Collaborative Research
Smith-McCort dysplasia 1
rareAny Smith-McCort dysplasia in which the cause of the disease is a mutation in the DYM gene.
- Identifiers
- MONDO:0011814 OMIM:607326
- Causal genes
- DYM
- Part of
- Smith-McCort dysplasia
- Also known as
- DYM Smith-McCort dysplasia · SMC · Smc1 · Smith-McCort dysplasia caused by mutation in DYM · Smith-McCort dysplasia type 1
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