Term Name: | Meier-Gorlin syndrome 3 |
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Synonyms: | |
Definition: | A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC6 gene on chromosome 16q11. |
Ontology: | Human Disease [DOID:0080514] ( DOID:0080514 ) |