Cat Breeds

- 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 Gangliosidosi

- 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 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

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