Seckel syndrome 10 Disease Ontology Browser

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Seckel syndrome 10 (DOID:0070008)
Alliance: disease page
Synonyms: SCKL10
Alt IDs: OMIM:617253
Definition: A Seckel syndrome that has_material_basis_in compound heterozygous mutation in the NSMCE2 gene on chromosome 8q24.

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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