Seckel syndrome 1 Disease Ontology Browser

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Disease Ontology Browser

Seckel syndrome 1 (DOID:0070007)
Alliance: disease page
Synonyms: microcephalic primordial dwarfism I; SCKL1
Alt IDs: OMIM:210600, MESH:C537533
Definition: A Seckel syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ATR gene on chromosome 3q23.

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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