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Meier-Gorlin syndrome 3

MONDO:0013430

Any Meier-Gorlin syndrome in which the cause of the disease is a mutation in the ORC6 gene.

Also known as: Meier-Gorlin syndrome 3, Meier-Gorlin syndrome caused by mutation in ORC6, Meier-Gorlin syndrome type 3, ORC6 Meier-Gorlin syndrome, MGORS3, Meier-GORLIN syndrome 3

0 clinical trials for this condition and its sub-types, 0 tagged with Meier-Gorlin syndrome 3 itself.

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