Search Ontology:
Human Disease

visceral heterotaxy 14

Term ID
DOID:0061123
Synonyms
Definition
A visceral heterotaxy that has_material_basis_in homozygous or compound heterozygous mutation in the C1ORF127 gene on chromosome 1p36. https://pubmed.ncbi.nlm.nih.gov/39513328/
References
Ontology
Human Disease   ( DOID:0061123 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models