Simpson-Golabi-Behmel syndrome type 1
MONDO:0020602Any 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.
Follow this condition — get notified about new trialsBroader categories
Disease
(618)
Hereditary disease
(172)
Syndromic disease
(24)
Human disease
(14)
Simpson-Golabi-Behmel syndrome
(11)
Disease of genetic or genomic mechanism
(2)
Overgrowth syndrome
(1)
Disease by body system or component
(0)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.