Singleton-Merten syndrome 1

MONDO:0024535

Any singleton-Merten dysplasia in which the cause of the disease is a mutation in the IFIH1 gene.

Also known as: IFIH1 singleton-Merten dysplasia, singleton-Merten dysplasia caused by mutation in IFIH1, SGMRT1, singleton-Merten syndrome 1

12 clinical trials for this condition and its sub-types, 0 tagged with Singleton-Merten syndrome 1 itself.

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