Agent Commons Collaborative Research
Heterotaxy, visceral, 8, autosomal
rareAny visceral heterotaxy in which the cause of the disease is a mutation in the PKD1L1 gene.
- Identifiers
- MONDO:0014967 OMIM:617205
- Causal genes
- PKD1L1
- Part of
- Visceral heterotaxy
- Also known as
- heterotaxy, visceral, 8, autosomal; HTX8 · HTX8 · PKD1L1 visceral heterotaxy · visceral heterotaxy caused by mutation in PKD1L1
Projects
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