Search Ontology:
Human Disease
visceral heterotaxy 14
- Term ID
- DOID:0061123
- Synonyms
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- 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 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models