Cat Breed Library

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 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