periventricular nodular heterotopia 8 Disease Ontology Browser

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Disease Ontology Browser

periventricular nodular heterotopia 8 (DOID:0061245)
Alliance: disease page
Alt IDs: OMIM:618185
Definition: A congenital nervous system abnormality characterized by abnormal neuronal migration during brain development, resulting in delayed psychomotor development that has_material_basis_in heterozygous mutation in the ARF1 gene on chromosome 1q42.

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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