right atrial isomerism

Summary
Synonym
  • Ivemark syndrome
  • asplenia with cardiovascular anomalies
Definition
A visceral heterotaxy that is characterized by complete atrioventricular septal defect with a common atrium and univentricular AV connection, total anomalous pulmonary drainage, and transposition or malposition of the great arteries and that has_material_basis_in homozygous mutation in the GDF1 gene on chromosome 19p12.
Super Class
autosomal recessive disease visceral heterotaxy
External Links
Disease Ontology
DOID:0060856
Mondo Disease Ontology
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
55997 CFC1 cryptic, EGF-CFC family member 1
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
P0CG37 Cryptic protein

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024