Heterotaxy, visceral, 7, autosomal

Any visceral heterotaxy in which the cause of the disease is a mutation in the MMP21 gene.

Also known as: HTX7, MMP21 visceral heterotaxy, heterotaxy, visceral, 7, autosomal, heterotaxy, visceral, 7, autosomal; HTX7, visceral heterotaxy caused by mutation in MMP21

1 clinical trial for this condition and its sub-types, 0 tagged with Heterotaxy, visceral, 7, autosomal itself.