FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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Term visceral heterotaxy 6 ID (Ontology) DOID:0051020 (Human Disease)
Definition A visceral heterotaxy that is has_material_basis_in homozygous mutation in the CCDC11 gene (CFAP53) on chromosome 18q21.
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 Genes
 visceral heterotaxy 6       1
 for disease ribbon | visceral heterotaxy 6       1
 model of | visceral heterotaxy 6       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
physical disorder                |
 |__visceral heterotaxy__________|
                                 visceral heterotaxy 6  1 rec.
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Is a visceral heterotaxy
autosomal recessive disease
Part of
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MIM:614779