Search Ontology:
Human Disease

visceral heterotaxy 13

Term ID
DOID:0051027
Synonyms
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/
References
Ontology
Human Disease   ( DOID:0051027 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models