Seckel syndrome 6 Disease Ontology Browser

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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 Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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