Visceral heterotaxy
MONDO:0018677A rare, genetic disorder in which symptoms are generally secondary to the abnormal location of the organs within the thoracic, abdominal, or peritoneal cavities. Anatomic and functional problems can include cardiac defects, intestinal malrotation leading to volvulus, biliary atresia, and various defects of the central nervous system, urinary tract, and skeleton.
Also known as: heterotaxia, heterotaxia syndrome, heterotaxy syndrome, heterotaxy, visceral, incomplete situs inversus, lateralization defect, partial situs inversus, situs ambiguous
2 clinical trials for this condition and its sub-types.
Follow this condition to get notified about new trialsSub-types
Dextrocardia
(1)
Situs inversus
(1)
Heterotaxy, visceral, 10, autosomal, with male infertility
(0)
Heterotaxy, visceral, 11, autosomal, with male infertility
(0)
Heterotaxy, visceral, 12, autosomal
(0)
Heterotaxy, visceral, 13, autosomal
(0)
Heterotaxy, visceral, 14, autosomal
(0)
Heterotaxy, visceral, 1, X-linked
(0)
Heterotaxy, visceral, 2, autosomal
(0)
Heterotaxy, visceral, 3, autosomal
(0)
Heterotaxy, visceral, 4, autosomal
(0)
Heterotaxy, visceral, 5, autosomal
(0)
Heterotaxy, visceral, 6, autosomal
(0)
Heterotaxy, visceral, 7, autosomal
(0)
Heterotaxy, visceral, 8, autosomal
(0)
Heterotaxy, visceral, 9, autosomal, with male infertility
(0)
Laterality defects, autosomal dominant
(0)
Levocardia
(0)
Right atrial isomerism
(0)
Situs inversus totalis with cystic dysplasia of kidneys and pancreas
(0)
Broader categories
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)
Disease by body system or component
(0)
Disease by developmental or physiological process
(0)