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Hémophilie A (Boxer, gène F8)
PRA1, Atrophie rétienne progressive 1 (Papillon, gène CNGB1)
Syndrome myasthénique congénital (Golden Retriever, gène COLQ)
Pyruvate Kinase Deficiency (PKD) – Pug
Déficit en pyruvate kinase (PKD) - Beagle
Neuronal Ceroid Lipofuscinosis 6 (NCL-6, CLN6) - Australian Shepherd
Cycling Neutropenia (CN, AP3B1 Gene)
Congenital Myotonia – Australian Cattle Dog Type
Intestinal Cobalamin (Vitamin B12) Malabsorption (CUBN Gene)
A Locus (Agouti: Yellow/Sable/Red, Recessive Black)
Hyperekplexia (Startle Disease) – Australian Shepherd
Copper toxicosis - labrador retriever
Copper toxicosis - Doberman Pinscher
Cerebellar Degeneration-Myositis Complex (CDMC) SLC25A12 Gene
CP1-Cleft Palate 1,DLX6 Gene - Nova Scotia Duck Tolling Retriever
Cystinuria Type 3, Bulldog And Mastiff (Cyst3, SLC3A1, SLC7A9)
Factor VII Deficiency (F7)
Leukocyte Adhesion Deficiency Type I (CLAD)- Irish Setter
Catalase Deficiency (CAT)
Prekallikrein Deficiency (KLKB1)
