OBO ID: DOID:0080514 |
Term Name: | Meier-Gorlin syndrome 3 | Search Ontology: | |
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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://www.omim.org/entry/613803 | ||
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Ontology: | Human Disease ( DOID:0080514 ) |
OTHER Meier-Gorlin syndrome 3 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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