Heterotaxy, visceral, 5, autosomal
MONDO:0700112Any visceral hetetotaxy in which the cause of the disease is a mutation in the NODAL gene.
Also known as: HTX5, NODAL visceral heterotaxy, SIV, situs inversus viscerum, visceral heterotaxy caused by mutation in NODAL
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)