Term Name: | Meier-Gorlin syndrome 4 |
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Synonyms: | |
Definition: | A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CDT1 gene on chromosome 16q24. |
Ontology: | Human Disease [DOID:0080515] ( DOID:0080515 ) |