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Cat Breed Library

Find the tests that matter 
for your breed.

You can find the most relevant tests included for your breed below 

(new tests are marked with '*' ):

A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z

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 Gangliosidosis

        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 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