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Disease Ontology Browser
Seckel syndrome 7 (DOID:0070011)
Alliance: disease page
Synonyms: SCKL7
Alt IDs: OMIM:614851
Definition: A Seckel syndrome that has_material_basis_in compound heterozygous mutation in the NIN gene on chromosome 14q22.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
02/05/2019
MGI 6.13
The Jackson Laboratory