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Metadata
ID	DOID:0051027
Name	visceral heterotaxy 13
Definition	A visceral heterotaxy that is characterized by heterotaxy and congenital heart disease and that has_material_basis_in homozygous mutation in the DAND5 gene on chromosome 19p13. https://pubmed.ncbi.nlm.nih.gov/36316122/
Xrefs	MIM:621079
Parent Relationships	is_a visceral heterotaxy is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance