DISEASE-DISEASE ASSOCIATIONS Disease,Disease,Common genes CADASIL,Infantile myofibromatosis,1 CADASIL,Early-onset autosomal dominant Alzheimer disease,(interactome association) CADASIL,Familial isolated dilated cardiomyopathy,(interactome association) CADASIL,Alagille syndrome due to 20p12 microdeletion,(interactome association) CADASIL,Alagille syndrome due to a JAG1 point mutation,(interactome association) CADASIL,Tetralogy of Fallot,(interactome association) CADASIL,Alobar holoprosencephaly,(interactome association) CADASIL,Lobar holoprosencephaly,(interactome association) CADASIL,Microform holoprosencephaly,(interactome association) CADASIL,Midline interhemispheric variant of holoprosencephaly,(interactome association) CADASIL,Semilobar holoprosencephaly,(interactome association) CADASIL,Septopreoptic holoprosencephaly,(interactome association) CADASIL,Chronic myeloid leukemia,(interactome association) CADASIL,Juvenile myelomonocytic leukemia,(interactome association) CADASIL,Noonan syndrome-like disorder with juvenile myelomonocytic leukemia,(interactome association) CADASIL,Precursor B-cell acute lymphoblastic leukemia,(interactome association) CADASIL,Precursor T-cell acute lymphoblastic leukemia,(interactome association) CADASIL,Synpolydactyly type 2,(interactome association) CADASIL,Xanthinuria type I,(interactome association) CADASIL,Adams-Oliver syndrome,(interactome association) CADASIL,Behavioral variant of frontotemporal dementia,(interactome association) CADASIL,Progressive non-fluent aphasia,(interactome association) CADASIL,Semantic dementia,(interactome association)