/heterotaxy, visceral, 7, autosomal

heterotaxy, visceral, 7, autosomal

Rare Disease

MONDO:0014762

Also Known As

HTX7MMP21 visceral heterotaxyheterotaxy, visceral, 7, autosomalheterotaxy, visceral, 7, autosomal; HTX7visceral heterotaxy caused by mutation in MMP21

Definition

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

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Associated Genes

MMP21 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:616749 ↗

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