Search Ontology:
Human Disease
Meier-Gorlin syndrome 3
- Term ID
- DOID:0080514
- Synonyms
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- Definition
- A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC6 gene on chromosome 16q11. https://pubmed.ncbi.nlm.nih.gov/37059840/
- References
- Ontology
- Human Disease ( DOID:0080514 )
- is a type of
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