Leydig cell hypoplasia, type 1
MONDO:0009384Any Leydig cell hypoplasia in which the cause of the disease is a mutation in the LHCGR gene.
Also known as: LHCGR Leydig cell hypoplasia, Leydig cell hypoplasia caused by mutation in LHCGR, leydig cell hypoplasia with hypergonadotropic hypogonadism, leydig cell hypoplasia with pseudohermaphroditism, Leydig cell Hypoplasia, type 2, Leydig cell agenesis, Leydig cell hypoplasia with male pseudohermaphroditism, Leydig cell hypoplasia, complete
0 clinical trials for this condition and its sub-types, 0 tagged with Leydig cell hypoplasia, type 1 itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Leydig cell hypoplasia, type 1
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.