/heterotaxy, visceral, 8, autosomal

heterotaxy, visceral, 8, autosomal

Rare Disease

MONDO:0014967

Also Known As

HTX8PKD1L1 visceral heterotaxyheterotaxy, visceral, 8, autosomalheterotaxy, visceral, 8, autosomal; HTX8visceral heterotaxy caused by mutation in PKD1L1

Definition

Any visceral heterotaxy in which the cause of the disease is a mutation in the PKD1L1 gene.

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Associated Genes

PKD1L1 ↗

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

External Resources

OMIM

OMIM:617205 ↗

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