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 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models