OBO ID: DOID:0080513 |
Term Name: | Meier-Gorlin syndrome 2 | Search Ontology: | |
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Definition: | A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC4 gene on chromosome 2q23. https://www.omim.org/entry/613800 | ||
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Ontology: | Human Disease ( DOID:0080513 ) |
OTHER Meier-Gorlin syndrome 2 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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