Search Ontology:
Human Disease
Meier-Gorlin syndrome 5
- Term ID
- DOID:0080516
- Synonyms
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- Definition
- A Meier-Gorlin syndrome that has_material_basis_in homozygous mutation in the CDC6 gene on chromosome 17q21. https://pubmed.ncbi.nlm.nih.gov/11477602/
- References
- Ontology
- Human Disease ( DOID:0080516 )
- is a type of
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Zebrafish Models