Heterotaxy, visceral, 5, autosomal

MONDO:0700112

Any visceral hetetotaxy in which the cause of the disease is a mutation in the NODAL gene.

Also known as: HTX5, NODAL visceral heterotaxy, SIV, situs inversus viscerum, visceral heterotaxy caused by mutation in NODAL

1 clinical trial for this condition and its sub-types, 0 tagged with Heterotaxy, visceral, 5, autosomal itself.

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