Search Ontology:
Human Disease

visceral heterotaxy 7

Term ID
DOID:0051021
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. https://pubmed.ncbi.nlm.nih.gov/26437028/
References
Ontology
Human Disease   ( DOID:0051021 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models
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