|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||any structural anomaly of the compact, white, heavily myelinated fiber bundle arising from the Ammon horn of the hippocampus in each cerebral hemisphere and projecting to the hypothalamus and the mammillary body (Mammalian Phenotype Ontology, MP_0003006)|
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3 gene mutations causing the abnormal hippocampal fornix morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.