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Included Health Tests by Cat Breed

Browse our cat breed database with 45+ health conditions. Search below to find the most notable conditions tested for your breed.
      • Progressive Retinal Atrophy (Discovered in the Abyssinian)
      • Pyruvate Kinase Deficiency
      • Hypertrophic Cardiomyopathy (Discovered in the Ragdoll)
      • Pyruvate Kinase Deficiency
      • Progressive Retinal Atrophy (Discovered in the Abyssinian)
      • Progressive Retinal Atrophy (Discovered in the Abyssinian)
      • Polycystic Kidney Disease (PKD)
      • Progressive Retinal Atrophy (Discovered in the Abyssinian)
      • Familial Episodic Hypokalemic Polymyopathy (Discovered in the Burmese)
      • Progressive Retinal Atrophy (Discovered in the Abyssinian)
      • Mucopolysaccharidosis Type VI
      • Mucopolysaccharidosis Type VI Modifier
      • Progressive Retinal Atrophy (Discovered in the Abyssinian)
      • Progressive Retinal Atrophy (Discovered in the Bengal)
      • Pyruvate Kinase Deficiency 
      • Hypotrichosis (Discovered in the Birman)
      • Familial Episodic Hypokalemic Polymyopathy (Discovered in the Burmese)
      • Autoimmune Lymphoproliferative Syndrome
      • Familial Episodic Hypokalemic Polymyopathy (Discovered in the Burmese)
      • Autoimmune Lymphoproliferative Syndrome
      • Familial Episodic Hypokalemic Polymyopathy
      • (Discovered in the Burmese)
      • Autoimmune Lymphoproliferative Syndrome
      • Familial Episodic Hypokalemic Polymyopathy (Discovered in the Burmese)
      •  Familial Episodic Hypokalemic Polymyopathy (Discovered in the Burmese)
      • Burmese Head Defect (Discovered in the Burmese)
      • GM2 Gangliosidosis Type II (Discovered in the Burmese)
      •  Mucopolysaccharidosis Type VI
      • Pyruvate Kinase Deficiency
      •  Progressive Retinal Atrophy (Discovered in the Abyssinian)
      • Progressive Retinal Atrophy (Discovered in the Abyssinian)
      • Congenital Myasthenic Syndrome (Discovered in the Devon Rex and Sphynx
      • GM2 Gangliosidosis
      • Hyperoxaluria Type II
      • Lipoprotein Lipase Deficiency
      • Cystinuria Type 1A, Factor XII Deficiency (Variant 2)
      • Factor XII Deficiency (Variant 1)
      • Sphingomyelinosis (Variant 2)
      • Mucopolysaccharidosis Type VII (Variant 1)
      • MDR1 Medication Sensitivity
      • Dihydropyrimidinase Deficiency
      • Cystinuria Type B (Variant 2)
      • Acute Intermittent Porphyria (Variant 1)
      • Mucopolysaccharidosis Type VI
      • Hemophilia B (Variant 1)
      • GM2 Gangliosidosis Type II (Discovered in Domestic Shorthair cats)
      • GM1 Gangliosidosis
      • Mucopolysaccharidosis Type VII (Variant 2)
      • Cystinuria Type B (Variant 1)
      • Congenital Erythropoietic Porphyria
      • Sphingomyelinosis (Variant 1), Polycystic Kidney Disease (PKD)
      • Glutaric Aciduria Type II
      • Acute Intermittent Porphyria (Variant 5)
      • Mucopolysaccharidosis Type I
      • Congenital Adrenal Hyperplasia
      • Myotonia Congenita
      • Vitamin D-Dependent Rickets
      • Hemophilia B (Variant 2)
      • Cystinuria Type B (Variant 3)
      • Acute Intermittent Porphyria (Variant 2)
      • Pyruvate Kinase Deficiency
      • Mucopolysaccharidosis Type VI Modifier 
      • GM2 Gangliosidosis
      • Hyperoxaluria Type II
      • Lipoprotein Lipase Deficiency
      • Cystinuria Type 1A
      • Factor XII Deficiency (Variant 2)
      • Factor XII Deficiency (Variant 1)
      • Sphingomyelinosis (Variant 2)
      • Mucopolysaccharidosis Type VII (Variant 1)
      • MDR1 Medication Sensitivity, Dihydropyrimidinase Deficiency
      • Cystinuria Type B (Variant 2)
      • Acute Intermittent Porphyria (Variant 1)
      • Mucopolysaccharidosis Type VI
      • Hemophilia B (Variant 1)
      • GM2 Gangliosidosis Type II (Discovered in Domestic Shorthair cats)
      • GM1 Gangliosidosis
      • Mucopolysaccharidosis Type VII (Variant 2)
      • Cystinuria Type B (Variant 1)
      • Congenital Erythropoietic Porphyria
      • Sphingomyelinosis (Variant 1)
      • Polycystic Kidney Disease (PKD)
      • Glutaric Aciduria Type II
      • Acute Intermittent Porphyria (Variant 5)
      • Mucopolysaccharidosis Type I
      • Congenital Adrenal Hyperplasia
      • Myotonia Congenita
      • Vitamin D-Dependent Rickets
      • Hemophilia B (Variant 2)
      • Cystinuria Type B (Variant 3)
      • Acute Intermittent Porphyria (Variant 2)
      • Pyruvate Kinase Deficiency
      • Mucopolysaccharidosis Type VI Modifier
      • GM2 Gangliosidosis, Hyperoxaluria Type II
      • Lipoprotein Lipase Deficiency
      • Cystinuria Type 1A
      • Factor XII Deficiency (Variant 2)
      • Factor XII Deficiency (Variant 1)
      • Sphingomyelinosis (Variant 2)
      • Mucopolysaccharidosis Type VII (Variant 1)
      • MDR1 Medication Sensitivity
      • Dihydropyrimidinase Deficiency
      • Cystinuria Type B (Variant 2)
      • Acute Intermittent Porphyria (Variant 1)
      • Mucopolysaccharidosis Type VI
      • Hemophilia B (Variant 1), GM2 Gangliosidosis Type II (Discovered in Domestic Shorthair cats)
      • GM1 Gangliosidosis
      • Mucopolysaccharidosis Type VII (Variant 2)
      • Cystinuria Type B (Variant 1)
      • Congenital Erythropoietic Porphyria
      • Sphingomyelinosis (Variant 1)
      • Polycystic Kidney Disease (PKD),
      • Glutaric Aciduria Type II
      • Acute Intermittent Porphyria (Variant 5)
      • Mucopolysaccharidosis Type I
      • Congenital Adrenal Hyperplasia
      • Myotonia Congenita
      • Vitamin D-Dependent Rickets
      • Hemophilia B (Variant 2)
      • Cystinuria Type B (Variant 3)
      • Acute Intermittent Porphyria (Variant 2)
      • Pyruvate Kinase Deficiency
      • Mucopolysaccharidosis Type VI Modifier
      • GM2 Gangliosidosis
      • Hyperoxaluria Type II
      • Lipoprotein Lipase Deficiency
      • Cystinuria Type 1A
      • Factor XII Deficiency (Variant 2)
      • Sphingomyelinosis (Variant 2)
      • Mucopolysaccharidosis Type VII (Variant 1)
      • MDR1 Medication Sensitivity
      • Dihydropyrimidinase Deficiency
      • Cystinuria Type B (Variant 2)
      • Acute Intermittent Porphyria (Variant 1)
      • Mucopolysaccharidosis Type VI
      • Hemophilia B (Variant 1)
      • GM2 Gangliosidosis Type II (Discovered in Domestic Shorthair cats)
      • GM1 Gangliosidosis
      • Mucopolysaccharidosis Type VII (Variant 2)
      • Cystinuria Type B (Variant 1)
      • Congenital Erythropoietic Porphyria
      • Sphingomyelinosis (Variant 1)
      • Polycystic Kidney Disease (PKD)
      • Glutaric Aciduria Type II
      • Acute Intermittent Porphyria (Variant 5)
      • Mucopolysaccharidosis Type I
      • Congenital Adrenal Hyperplasia
      • Myotonia Congenita
      • Vitamin D-Dependent Rickets
      • Hemophilia B (Variant 2)
      • Cystinuria Type B (Variant 3)
      • Acute Intermittent Porphyria (Variant 2)
      • Pyruvate Kinase Deficiency
      • Mucopolysaccharidosis Type VI Modifier
      • GM2 Gangliosidosis
      • Hyperoxaluria Type II
      • Lipoprotein Lipase Deficiency
      • Cystinuria Type 1A
      • Factor XII Deficiency (Variant 2)
      • Sphingomyelinosis (Variant 2)
      • Mucopolysaccharidosis Type VII (Variant 1)
      • MDR1 Medication Sensitivity
      • Dihydropyrimidinase Deficiency
      • Cystinuria Type B (Variant 2)
      • Acute Intermittent Porphyria (Variant 1)
      • Mucopolysaccharidosis Type VI
      • Hemophilia B (Variant 1)
      • GM2 Gangliosidosis Type II (Discovered in Domestic Shorthair cats)
      • GM1 Gangliosidosis
      • Mucopolysaccharidosis Type VII (Variant 2)
      • Cystinuria Type B (Variant 1)
      • Congenital Erythropoietic Porphyria
      • Sphingomyelinosis (Variant 1)
      • Polycystic Kidney Disease (PKD)
      • Glutaric Aciduria Type II
      • Acute Intermittent Porphyria (Variant 5)
      • Mucopolysaccharidosis Type I
      • Congenital Adrenal Hyperplasia
      • Myotonia Congenita
      • Vitamin D-Dependent Rickets
      • Hemophilia B (Variant 2)
      • Cystinuria Type B (Variant 3)
      • Acute Intermittent Porphyria (Variant 2)
      • Pyruvate Kinase Deficiency
      • Mucopolysaccharidosis Type VI Modifier
      • GM2 Gangliosidosis
      • Hyperoxaluria Type II
      • Lipoprotein Lipase Deficiency
      • Cystinuria Type 1A
      • Factor XII Deficiency (Variant 2)
      • Sphingomyelinosis (Variant 2)
      • Mucopolysaccharidosis Type VII (Variant 1)
      • MDR1 Medication Sensitivity
      • Dihydropyrimidinase Deficiency
      • Cystinuria Type B (Variant 2)
      • Acute Intermittent Porphyria (Variant 1)
      • Mucopolysaccharidosis Type VI
      • Hemophilia B (Variant 1)
      • GM2 Gangliosidosis Type II (Discovered in Domestic Shorthair cats
      • GM1 Gangliosidosis
      • Mucopolysaccharidosis Type VII (Variant 2)
      • Cystinuria Type B (Variant 1)
      • Congenital Erythropoietic Porphyria
      • Sphingomyelinosis (Variant 1)
      • Polycystic Kidney Disease (PKD)
      • Glutaric Aciduria Type II, Acute Intermittent Porphyria (Variant 5)
      • Mucopolysaccharidosis Type I
      • Congenital Adrenal Hyperplasia
      • Myotonia Congenita
      • Vitamin D-Dependent Rickets
      • Hemophilia B (Variant 2)
      • Cystinuria Type B (Variant 3)
      • Acute Intermittent Porphyria (Variant 2)
      • Pyruvate Kinase Deficiency
      • Mucopolysaccharidosis Type VI Modifier
      • Pyruvate Kinase Deficiency
      • Pyruvate Kinase Deficiency
      • Polycystic Kidney Disease (PKD)
      • Progressive Retinal Atrophy (Discovered in the Bengal)
      • Pyruvate Kinase Deficiency
      • Factor XII Deficiency (Variant 1)
      • Factor XII Deficiency (Variant 2)
      • Polycystic Kidney Disease (PKD)
      • GM2 Gangliosidosis Type II (Discovered in Japanese domestic cats)
      • GM1 Gangliosidosis
      • Pyruvate Kinase Deficiency
      • Pyruvate Kinase Deficiency
      • Pyruvate Kinase Deficiency
      • Factor XII Deficiency (Variant 2)
      • Factor XII Deficiency (Variant 1)
      • MDR1 Medication Sensitivity
      • Spinal Muscular Atrophy (Discovered in the Maine Coon)
      • Hypertrophic Cardiomyopathy (Discovered in the Maine Coon)
      • Cystinuria Type B (Variant 3)
      • Pyruvate Kinase Deficiency
      • Factor XII Deficiency (Variant 2)
      • Factor XII Deficiency (Variant 1)
      • MDR1 Medication Sensitivity
      • Spinal Muscular Atrophy (Discovered in the Maine Coon)
      • Hypertrophic Cardiomyopathy (Discovered in the Maine Coon)
      • Cystinuria Type B (Variant 3)
      • Pyruvate Kinase Deficiency
      • Factor XII Deficiency (Variant 1)
      • Factor XII Deficiency (Variant 2)
      • Progressive Retinal Atrophy (Discovered in the Abyssinian) 
      • Factor XII Deficiency (Variant 1)
      • Factor XII Deficiency (Variant 2)
      • Pyruvate Kinase Deficiency
      • Progressive Retinal Atrophy (Discovered in the Abyssinian)
      • Progressive Retinal Atrophy (Discovered in the Abyssinian)
      • Pyruvate Kinase Deficiency
      • Polycystic Kidney Disease (PKD)
      • Glycogen Storage Disease (Discovered in the Norwegian Forest Cat)
      • Pyruvate Kinase Deficiency
      • Progressive Retinal Atrophy (Discovered in the Abyssinian)
      • Mucopolysaccharidosis Type VI
      • Progressive Retinal Atrophy (Discovered in the Abyssinian)
      • Progressive Retinal Atrophy (Discovered in the Abyssinian)
      • Polycystic Kidney Disease (PKD)
      • Chediak-Higashi Syndrome (Discovered in the Persian)
      • Progressive Retinal Atrophy (Discovered in the Abyssinian)
      • Pyruvate Kinase Deficiency
      • Hypertrophic Cardiomyopathy (Discovered in the Maine Coon)
      • Progressive Retinal Atrophy (Discovered in the Abyssinian)
      • Hypertrophic Cardiomyopathy (Discovered in the Ragdoll)
      • Polycystic Kidney Disease (PKD)
      • Hypertrophic Cardiomyopathy (Discovered in the Ragdoll)
      • Pyruvate Kinase Deficiency
      • Earfold and Osteochondrodysplasia (Discovered in the Scottish Fold), Polycystic Kidney Disease (PKD)
      • Earfold and Osteochondrodysplasia (Discovered in the Scottish Fold)
      • Polycystic Kidney Disease (PKD)
      • Polycystic Kidney Disease (PKD)
      • Polycystic Kidney Disease (PKD)
      • Progressive Retinal Atrophy (Discovered in the Abyssinian)
      • Mucopolysaccharidosis Type VI
      • GM1 Gangliosidosis
      • Acute Intermittent Porphyria (Variant 4)
      • Polycystic Kidney Disease (PKD)
      • Acute Intermittent Porphyria (Variant 3)
      • Mucopolysaccharidosis Type VI Modifier
      • Pyruvate Kinase Deficiency
      • Polycystic Kidney Disease (PKD)
      • Progressive Retinal Atrophy (Discovered in the Abyssinian)
      • Pyruvate Kinase Deficiency
      • Progressive Retinal Atrophy (Discovered in the Abyssinian)
      • Pyruvate Kinase Deficiency
      • Congenital Myasthenic Syndrome (Discovered in the Devon Rex and Sphynx)
      • Cystinuria Type B (Variant 3)
      • GM1 Gangliosidosis
      • Familial Episodic Hypokalemic Polymyopathy (Discovered in the Burmese)
      • Progressive Retinal Atrophy (Discovered in the Abyssinian)
      • Familial Episodic Hypokalemic Polymyopathy (Discovered in the Burmese)
      • Pyruvate Kinase Deficiency