Meier-Gorlin syndrome 6
MONDO:0014794Any Meier-Gorlin syndrome in which the cause of the disease is a mutation in the GMNN gene.
Also known as: GMNN Meier-Gorlin syndrome, MGORS6, Meier-Gorlin syndrome 6, Meier-Gorlin syndrome caused by mutation in GMNN, Meier-Gorlin syndrome type 6, Meier-GORLIN syndrome 6
0 clinical trials for this condition and its sub-types, 0 tagged with Meier-Gorlin syndrome 6 itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Part of
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.