|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||any structural anomaly of the ependyma-lined lumen of the spinal cord that is filled with cerebrospinal fluid; it is patent with the ventricular system of the brain and frequently becomes occluded in aging adults (Mammalian Phenotype Ontology, MP_0009688)|
|Downloads & Tools|
3 gene mutations causing the abnormal spinal cord central canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.