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Disease Ontology Browser
Seckel syndrome 9 (DOID:0070005)
Alliance: disease page
Synonyms: SCKL9
Alt IDs: OMIM:616777
Definition: A Seckel syndrome that has_material_basis_in homozygous mutation in the TRAIP gene on chromosome 3p21.


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
04/16/2024
MGI 6.23
The Jackson Laboratory