GCh, Ch, JCh Karady Evermore Golden Touch

 Collie Eye Anomaly (CEA): N/CEA

MDR1 gene variant: N/N (+/+) 

Degenerative Myelopathy: N/N

Progressive Retinal Atrophy (CNGA1-PRA): N/N 

Progressive Retinal Atrophy (BBS2-PRA): N/N

von Willebrand disease type III (vWD3): N/N

Dermatomyositis (DMS): Low risk (AabbCC)

Chondrodysplasia (CDPA): N/N 

Chondrodystrophy (CDDY and IVDD risk): N/N 

Gallbladder Mucoceles (GBM): N/N 

Hyperuricosuria (HUU): N/N 

Malignant Hyperthermia (MH): N/N 

Paroxysmal Exercise-Induced Dyskinesia (PED): N/N

Polydactyly (PPD): N/N 

Progressive Retinal Atrophy (prcd-PRA): N/N 

von Willebrand disease type I (vWD1): N/N 

S locus: N/N (no white factor)

 Hip Dysplasia (HD): A/A

 Elbow Dysplasia (ED): 0/0 

Patella Luxation: free