Holoprosencephaly 13, X-linked Disease Ontology Browser

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Disease Ontology Browser

Holoprosencephaly 13, X-linked (DOID:0060954)
Alliance: disease page
Alt IDs: OMIM:301043
Definition: A holoprosencephaly characterized by midline developmental defects that mainly affect the brain and craniofacial structure that has_material_basis_in heterozygous mutation in the STAG2 gene on chromosome Xq25.

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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