|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||an abnormal communication between the terminus of a coronary artery, bypassing the myocardial capillary bed and entering a chamber of the heart (coronary-cameral fistula) (Mammalian Phenotype Ontology, MP_0011657)|
|Downloads & Tools|
1 gene mutations causing the coronary-cameral fistula phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
|SMARCA4||SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4|