Heterotaxy, visceral, 7, autosomal

MONDO:0014762

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

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