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Disease Ontology Browser
Seckel syndrome 6 (DOID:0070006)
Alliance: disease page
Synonyms: SCKL6
Alt IDs: OMIM:614728
Definition: A Seckel syndrome that has_material_basis_in homozygous mutation in the CEP63 gene on chromosome 3q22.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory