abnormal orbitofrontal cortex morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the region of the cerebral cortex covering the basal surface of the frontal lobes; this region normally controls emotion and decision making (Mammalian Phenotype Ontology, MP_0004170)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004170
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1 gene mutations causing the abnormal orbitofrontal cortex morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
MECP2 methyl CpG binding protein 2