Seckel syndrome 9 Disease Ontology Browser

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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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