For your breed
All MyCatDNA tests include:
- Results for over 40 genetic diseases.
- Testing for 20+ traits including coat colors, coat types, and morphology
- Genetic determination of blood types A, B, and AB
- Genetic diversity information
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You can find the most relevant tests included for your breed below:
| Abyssinian |
Progressive Retinal Atrophy (Discovered in the Abyssinian), Pyruvate Kinase Deficiency |
| American Bobtail | Hypertrophic Cardiomyopathy (Discovered in the Ragdoll), Pyruvate Kinase Deficiency |
|
American Curl Longhair |
Progressive Retinal Atrophy (Discovered in the Abyssinian) |
|
American Curl Shorthair |
Progressive Retinal Atrophy (Discovered in the Abyssinian) |
|
American Shorthair |
Polycystic Kidney Disease (PKD) |
|
American Wirehair |
Progressive Retinal Atrophy (Discovered in the Abyssinian) |
|
Australian Mist |
Familial Episodic Hypokalemic Polymyopathy (Discovered in the Burmese) |
|
Balinese |
Progressive Retinal Atrophy (Discovered in the Abyssinian), Mucopolysaccharidosis Type VI, Mucopolysaccharidosis Type VI Modifier |
|
Bengal |
Progressive Retinal Atrophy (Discovered in the Abyssinian), Progressive Retinal Atrophy (Discovered in the Bengal), Pyruvate Kinase Deficiency |
|
Birman |
Hypotrichosis (Discovered in the Birman) |
|
Bombay |
Familial Episodic Hypokalemic Polymyopathy (Discovered in the Burmese) |
|
British Longhair |
Autoimmune Lymphoproliferative Syndrome, Familial Episodic Hypokalemic Polymyopathy (Discovered in the Burmese) |
|
British Mediumhair |
Autoimmune Lymphoproliferative Syndrome, Familial Episodic Hypokalemic Polymyopathy (Discovered in the Burmese) |
|
British Shorthair |
Autoimmune Lymphoproliferative Syndrome, Familial Episodic Hypokalemic Polymyopathy (Discovered in the Burmese) |
|
Burmese |
Familial Episodic Hypokalemic Polymyopathy (Discovered in the Burmese), Burmese Head Defect (Discovered in the Burmese), GM2 Gangliosidosis Type II (Discovered in the Burmese) |
|
Chartreux |
Mucopolysaccharidosis Type VI, Polycystic Kidney Disease (PKD) |
| Chausie | Pyruvate Kinase Deficiency |
|
Colorpoint Shorthair |
Progressive Retinal Atrophy (Discovered in the Abyssinian) |
| Cornish Rex |
Progressive Retinal Atrophy (Discovered in the Abyssinian) |
| Devon Rex |
Congenital Myasthenic Syndrome (Discovered in the Devon Rex and Sphynx |
| Domestic Cat |
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 |
| Domestic Cat (European) |
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 |
| Domestic Cat (US) |
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 |
| Domestic Longhair |
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 |
| Domestic Mediumhair |
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 |
| Domestic Shorthair |
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 |
| Egyptian Mau |
Pyruvate Kinase Deficiency |
| European Shorthair |
Pyruvate Kinase Deficiency |
| Exotic Shorthair |
Polycystic Kidney Disease (PKD) |
| Highlander | Progressive Retinal Atrophy (Discovered in the Bengal), Pyruvate Kinase Deficiency |
| Himalayan | Factor XII Deficiency (Variant 1), Factor XII Deficiency (Variant 2) |
| Irish shorthair |
Polycystic Kidney Disease (PKD) |
| Japanese Shorthair |
GM2 Gangliosidosis Type II (Discovered in Japanese domestic cats) |
| Korat |
GM1 Gangliosidosi |
| LaPerm |
Pyruvate Kinase Deficiency |
| LaPerm Shorthair |
Pyruvate Kinase Deficiency |
| Lykoi | Pyruvate Kinase Deficiency |
| Maine Coon |
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 |
| Maine Coon Polydactyl |
Factor XII Deficiency (Variant 2), Factor XII Deficiency (Variant 1), MDR1Medication Sensitivity, Spinal Muscular Atrophy (Discovered in the Maine Coon), Hypertrophic Cardiomyopathy (Discovered in the Maine Coon), Cystinuria Type B (Variant 3), Pyruvate Kinase Deficiency |
| Manx | Factor XII Deficiency (Variant 1), Factor XII Deficiency (Variant 2), Progressive Retinal Atrophy (Discovered in the Abyssinian) |
| Minuet |
Factor XII Deficiency (Variant 1),
Factor XII Deficiency (Variant 2), Pyruvate Kinase Deficiency
|
| Munchkin |
Progressive Retinal Atrophy (Discovered in the Abyssinian) |
| Munchkin Longhair |
Progressive Retinal Atrophy (Discovered in the Abyssinian) |
| Neva Masquerade |
Pyruvate Kinase Deficiency, Polycystic Kidney Disease (PKD) |
| Norwegian Forest Cat |
Glycogen Storage Disease (Discovered in the Norwegian Forest Cat), Pyruvate Kinase Deficiency |
| Ocicat |
Progressive Retinal Atrophy (Discovered in the Abyssinian), Mucopolysaccharidosis Type VI |
| Oriental Longhair |
Progressive Retinal Atrophy (Discovered in the Abyssinian) |
| Oriental Shorthair |
Progressive Retinal Atrophy (Discovered in the Abyssinian) |
| Persian |
Polycystic Kidney Disease (PKD), Chediak-Higashi Syndrome (Discovered in the Persian), Progressive Retinal Atrophy (Discovered in the Persian) |
| Peterbald |
Progressive Retinal Atrophy (Discovered in the Abyssinian) |
| Pixiebob |
Pyruvate Kinase Deficiency, Hypertrophic Cardiomyopathy (Discovered in the Maine Coon), Progressive Retinal Atrophy (Discovered in the Abyssinian) |
| Ragdoll |
Hypertrophic Cardiomyopathy (Discovered in the Ragdoll), Polycystic Kidney Disease (PKD) |
| Ragamuffin |
Hypertrophic Cardiomyopathy (Discovered in the Ragdoll) |
| Savannah |
Pyruvate Kinase Deficiency |
| Scottish Fold Longhair |
Earfold and Osteochondrodysplasia (Discovered in the Scottish Fold), Polycystic Kidney Disease (PKD) |
| Scottish Fold Shorthair |
Earfold and Osteochondrodysplasia (Discovered in the Scottish Fold), Polycystic Kidney Disease (PKD) |
| Scottish Straight |
Polycystic Kidney Disease (PKD) |
| Scottish Straight Longhair |
Polycystic Kidney Disease (PKD) |
| Siamese |
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 |
| Siberian |
Pyruvate Kinase Deficiency, Polycystic Kidney Disease (PKD) |
| Singapura |
Progressive Retinal Atrophy (Discovered in the Abyssinian), Pyruvate Kinase Deficiency |
| Somali |
Progressive Retinal Atrophy (Discovered in the Abyssinian), Pyruvate Kinase Deficiency |
| Sphynx |
Congenital Myasthenic Syndrome (Discovered in the Devon Rex and Sphynx), Cystinuria Type B (Variant 3) |
| Thai Cat |
GM1 Gangliosidosis |
| Tiffanie |
Familial Episodic Hypokalemic Polymyopathy (Discovered in the Burmese) |
| Tonkinese |
Progressive Retinal Atrophy (Discovered in the Abyssinian), Familial Episodic Hypokalemic Polymyopathy (Discovered in the Burmese) |
| Toyger |
Pyruvate Kinase Deficiency |