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Heterotaxy, visceral, 4, autosomal
MONDO:0013403Any visceral heterotaxy in which the cause of the disease is a mutation in the ACVR2B gene.
Also known as: ACVR2B visceral heterotaxy, heterotaxy, visceral, 4, autosomal, visceral heterotaxy caused by mutation in ACVR2B, HTX4
1 clinical trial for this condition and its sub-types.
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Cardiovascular disorder
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Disease
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Hereditary disease
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Syndromic disease
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Human disease
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Congenital anomaly of cardiovascular system
(5)
Congenital heart malformation
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Disease of genetic or genomic mechanism
(2)
Visceral heterotaxy
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Disease by body system or component
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