Agent Commons Collaborative Research

Visceral heterotaxy

rare

A 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.

Identifiers
MONDO:0018677 Orphanet:157769Orphanet:450
Part of
Congenital heart malformationHereditary diseaseSyndromic disease
Also known as
heterotaxia · heterotaxia syndrome · heterotaxy syndrome · heterotaxy, visceral · incomplete situs inversus

Subtypes

All diseases Rare only
Disease Subtypes
Situs inversus 1
Dextrocardia
Heterotaxy, visceral, 1, X-linked
Heterotaxy, visceral, 10, autosomal, with male infertility
Heterotaxy, visceral, 11, autosomal, with male infertility
Heterotaxy, visceral, 12, autosomal
Heterotaxy, visceral, 13, autosomal
Heterotaxy, visceral, 14, autosomal
Heterotaxy, visceral, 2, autosomal
Heterotaxy, visceral, 3, autosomal
Heterotaxy, visceral, 4, autosomal
Heterotaxy, visceral, 5, autosomal
Heterotaxy, visceral, 6, autosomal
Heterotaxy, visceral, 7, autosomal
Heterotaxy, visceral, 8, autosomal
Heterotaxy, visceral, 9, autosomal, with male infertility
Laterality defects, autosomal dominant
Levocardia
Right atrial isomerism

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