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Disease Ontology Browser
Seckel syndrome 8 (DOID:0070009)
Alliance: disease page
Synonyms: SCKL8
Alt IDs: OMIM:615807
Definition: A Seckel syndrome that has_material_basis_in homozygous mutation in the DNA2 gene on chromosome 10q21.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
02/23/2021
MGI 6.16
The Jackson Laboratory