• 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
• 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 Gangliosidosis

• 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)
  • 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
• 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)
• 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

Included Health Tests

• Acute Intermittent Porphyria (Variant 1)
• Acute Intermittent Porphyria (Variant 2)
• Acute Intermittent Porphyria (Variant 3)
• Acute Intermittent Porphyria (Variant 4)
• Acute Intermittent Porphyria (Variant 5) - NEW!
• Autoimmune Lymphoproliferative Syndrome
• Blood Type
• Burmese Head Defect
• Chediak-Higashi Syndrome (Discovered in Persian cats) - NEW!
• Congenital Adrenal Hyperplasia
• Congenital Erythropoietic Porphyria
• Congenital Myasthenic Syndrome
• Cystinuria Type 1A
• Cystinuria Type B (Variant 1)
• Cystinuria Type B (Variant 2)
• Cystinuria Type B (Variant 3)
• Dihydropyrimidinase Deficiency
• Earfold and Osteochondrodysplasia (Discovered in the Scottish Fold)
• Factor XII Deficiency (Variant 1)
• Factor XII Deficiency (Variant 2) - NEW!
• Familial Episodic Hypokalaemic Polymyopathy (Discovered in Burmese)
• Glutaric Aciduria Type II - NEW!
• Glycogen Storage Disease
• GM1 Gangliosidosis
• GM2 Gangliosidosis
• GM2 Gangliosidosis, type II (Discovered in Burmese cats) - NEW!
• GM2 Gangliosidosis, type II (Discovered in domestic shorthair cats)
• GM2 Gangliosidosis, type II (Discovered in japanese domestic cats)
• Hemophilia B (Variant 1)
• Hemophilia B (Variant 2)
• Hyperoxaluria type II
• Hypertrophic Cardiomyopathy (Discovered in Maine Coon)
• Hypertrophic Cardiomyopathy (Discovered in Ragdoll)
• Hypotrichosis (Discovered in Sacred Birman)
• Lipoprotein Lipase Deficiency
• Mucopolysaccharidosis Type I
• Mucopolysaccharidosis Type VI (G1558A variant) - NEW!
• Mucopolysaccharidosis Type VI (T1427C variant)
• Mucopolysaccharidosis Type VII
• Mucopolysaccharidosis VII
• Multidrug Resistance 1
• Myotonia Congenita
• Polycystic Kidney Disease (PKD)
  
• Progressive Retinal Atrophy (Discovered in Bengal cats)
• Progressive Retinal Atrophy (rdAc-PRA)
• Pyruvate Kinase Deficiency
• Sphingomyelinosis (Variant 1)
• Sphingomyelinosis (Variant 2)
• Spinal Muscular Atrophy
• Vitamin D-Dependent Rickets

Included Trait Tests

Agouti (A) Locus:

• Charcoal (Apb)
• Non-Agouti (a)

Brown (B) Locus:

• Chocolate (b)
• Cinnamon (bl)
• Color (C) Locus:
• Colorpoint (cb)
• Colorpoint (cs)
• Mocha (cm) - NEW!
• Albinism (c)

Extension (E) Locus:

• Amber (e)
• Russet (er)

Dilution (D) Locus:

• Dilution (d)

White Patterns:

• Gloves (Birman - White feet)
• White Spotting/Dominant White

Other Coat Types:

• Glitter coat - NEW and EXCLUSIVE to Wisdom Health
• Hairlessness (Discovered in Sphynx)
• Long hair (mutation M1)
• Long hair (mutation M2)
• Long hair (mutation M3)
• Long hair (mutation M4)
• Lykoi coat (mutation Ca) - NEW!
• Lykoi coat (mutation VA) - NEW!
• Rexing (discovered in Cornish Rex and German Rex)
• Rexing (discovered in Devon Rex)

Body Features:

• Short tail (discovered in Japanese Bobtail cats)
• Short tail (discovered in Manx), two variants
• Polydactyly (mutation HW)
• Polydactyly (mutation UK1)
• Polydactyly (mutation UK2)