Heterotaxy, visceral, 4, autosomal

MONDO:0013403

Any visceral heterotaxy in which the cause of the disease is a mutation in the ACVR2B gene.

Also known as: ACVR2B visceral heterotaxy, heterotaxy, visceral, 4, autosomal, visceral heterotaxy caused by mutation in ACVR2B, HTX4

1 clinical trial for this condition and its sub-types, 0 tagged with Heterotaxy, visceral, 4, autosomal itself.

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