Search Ontology:
Human Disease
Meckel syndrome 9
- Term ID
- DOID:0061294
- Synonyms
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- Definition
- A Meckel syndrome that has_material_basis_in compound heterozygous mutation in the B9D1 gene on chromosome 17p11.2. https://pubmed.ncbi.nlm.nih.gov/21493627/
- References
- Ontology
- Human Disease ( DOID:0061294 )
Other Pages
Genes Involved
Zebrafish Models