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Metadata
ID	DOID:0051021
Name	visceral heterotaxy 7
Definition	A visceral heterotaxy that is characterized by complex congenital heart malformations and/or situs inversus and caused by defects in the normal left-right asymmetric positioning of internal organs and that has_material_basis_in homozygous or compound heterozygous mutation in the MMP21 gene on chromosome 10q26. https://pubmed.ncbi.nlm.nih.gov/26437028/
Xrefs	MIM:616749
Parent Relationships	is_a visceral heterotaxy is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance