Heterotaxy, visceral, 8, autosomal

Any visceral heterotaxy in which the cause of the disease is a mutation in the PKD1L1 gene.

Also known as: HTX8, PKD1L1 visceral heterotaxy, heterotaxy, visceral, 8, autosomal, heterotaxy, visceral, 8, autosomal; HTX8, visceral heterotaxy caused by mutation in PKD1L1

1 clinical trial for this condition and its sub-types, 0 tagged with Heterotaxy, visceral, 8, autosomal itself.