Term Name: visceral heterotaxy 7
Synonyms:
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.
Ontology: Human Disease [DOID:0051021]   ( DOID:0051021 )

Relationships
is a type of: autosomal recessive disease visceral heterotaxy