Adams-Oliver syndrome 1

Any Adams-Oliver syndrome in which the cause of the disease is a mutation in the ARHGAP31 gene.

Also known as: AOS1, ARHGAP31 Adams-Oliver syndrome, Adams-Oliver syndrome 1, Adams-Oliver syndrome caused by mutation in ARHGAP31, AOS, absence defect of limbs, scalp, and skull, aplasia cutis congenita with terminal transverse limb defects, aplasia cutis congenita, congenital heart defect, and frontonasal cysts

1 clinical trial for this condition and its sub-types, 0 tagged with Adams-Oliver syndrome 1 itself.