Simpson-Golabi-Behmel syndrome type 1

Any Simpson-Golabi-Behmel syndrome in which the cause of the disease is a mutation in the GPC3 gene.

Also known as: GPC3 Simpson-Golabi-Behmel syndrome, SGBS1, Simpson dysmorphia syndrome, Simpson-Golabi-Behmel syndrome caused by mutation in GPC3, Simpson-Golabi-Behmel syndrome, type 1, X-linked recessive, bulldog syndrome, Golabi-Rosen syndrome, Sgbs

0 clinical trials for this condition and its sub-types, 0 tagged with Simpson-Golabi-Behmel syndrome type 1 itself.