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autosomal visceral heterotaxy

MIM.605376 Chr.2

autosomal visceral heterotaxia

 

Synopsis

-  atrioventricular septal defect
-  mesocardia
-  left atrial isomerism

-  abdominal situs inversus (situs inversum viscerum, visceral heterotaxy)

Etiology

-  Ch.2: germline mutation in CFC1 gene encoding the CRYPTIC protein, on chromosome 2 (MIM.605194)
-  6q: Locus HTX3 (MIM.606325)

See also

-  situs inversus
-  X-linked visceral heterotaxy



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