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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