Heterotaxy, visceral, 8, autosomal

Definition

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

Also known as heterotaxy, visceral, 8, autosomal, heterotaxy, visceral, 8, autosomal; HTX8, HTX8, PKD1L1 visceral heterotaxy, visceral heterotaxy caused by mutation in PKD1L1 — per MONDO

Also identified as

• DOID 0051022 per MONDO
• OMIM 617205 per MONDO
• UMLS C4310668 per MONDO