Seckel syndrome 2 Disease Ontology Browser

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Disease Ontology Browser

Seckel syndrome 2 (DOID:0070013)
Alliance: disease page
Synonyms: microcephalic primordial dwarfism 2; SCKL2; Seckel-type dwarfism 2
Alt IDs: OMIM:606744, MESH:C537534
Definition: A Seckel syndrome that has_material_basis_in homozygous mutation in the RBBP8 gene on chromosome 18q11.

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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