A
-
- 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)
B
-
- 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)
C
-
- Mucopolysaccharidosis Type VI
-
- Pyruvate Kinase Deficiency
-
- Progressive Retinal Atrophy (Discovered in the Abyssinian)
-
- Progressive Retinal Atrophy (Discovered in the Abyssinian)
D
-
- 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
E
-
- Pyruvate Kinase Deficiency
-
- Pyruvate Kinase Deficiency
-
- Polycystic Kidney Disease (PKD)
H
-
- Progressive Retinal Atrophy (Discovered in the Bengal)
- Pyruvate Kinase Deficiency
-
- Factor XII Deficiency (Variant 1)
- Factor XII Deficiency (Variant 2)
I
-
- Polycystic Kidney Disease (PKD)
J
-
- GM2 Gangliosidosis Type II (Discovered in Japanese domestic cats)
K
-
- GM1 Gangliosidosi
L
-
- Pyruvate Kinase Deficiency
-
- Pyruvate Kinase Deficiency
-
- Pyruvate Kinase Deficiency
M
-
- 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)
N
-
- Pyruvate Kinase Deficiency
- Polycystic Kidney Disease (PKD)
-
- Glycogen Storage Disease (Discovered in the Norwegian Forest Cat)
- Pyruvate Kinase Deficiency
O
-
- Progressive Retinal Atrophy (Discovered in the Abyssinian)
- Mucopolysaccharidosis Type VI
-
- Progressive Retinal Atrophy (Discovered in the Abyssinian)
-
- Progressive Retinal Atrophy (Discovered in the Abyssinian)
P
-
- 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)
R
-
- Hypertrophic Cardiomyopathy (Discovered in the Ragdoll)
- Polycystic Kidney Disease (PKD)
-
- Hypertrophic Cardiomyopathy (Discovered in the Ragdoll)
S
-
- 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)
T
-
- 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