Heterotaxy, visceral, 8, autosomal
MONDO:0014967Any visceral heterotaxy in which the cause of the disease is a mutation in the PKD1L1 gene.
Also known as: HTX8, PKD1L1 visceral heterotaxy, heterotaxy, visceral, 8, autosomal, heterotaxy, visceral, 8, autosomal; HTX8, visceral heterotaxy caused by mutation in PKD1L1
1 clinical trial for this condition and its sub-types.
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Cardiovascular disorder
(1093)
Disease
(717)
Hereditary disease
(188)
Syndromic disease
(25)
Human disease
(15)
Congenital anomaly of cardiovascular system
(5)
Congenital heart malformation
(3)
Disease of genetic or genomic mechanism
(2)
Visceral heterotaxy
(1)
Disease by body system or component
(0)