All Breeding males and females have been genetically tested and are clear of the following genetic type and disorders:

Color tested

Blood Type Tested

Breed tested- Ragdoll

Hypertrophic Cardiomyopathy

Mucopolysaccharidosis type VI

Polycystic Kidney Disease

Acute Intermittent Porphyria, Variant 1, Variant 2, Variant 3, Variant 4, Variant 5, and Variant 6.

Alpha Mannosidosis

Autoimmune Lymphoproliferative Syndrome Brachycephaly

Congenital Adrenal-hyperplasia

Congenital Erythropoietic Porphyria, Variant 1 and Variant 2

Congenital Hypothyroidism

Congenital Myasthenic Syndrome

Cystinuria Type 1A, Type B, Variant 1, Type B, Variant 2, Type B, Variant 3, Type B, Variant 4, Type B, Variant 5.

Dihydropyrimidinase Deficiency

Epidermolysis Bullosa Simplex

Factor XII Deficiency Virant 1, Variant 2, and Variant 3.

Feline Immunodeficiency Virus (FIV) Infection Risk Modifier

Feline Leukocyte Adhesion Deficiency Type 1

Feline Niemann-Pick Disease

Feline Spongy Encephalopathy

Forebrain Commissural Malformation

Gangliosidosis GM2A

Glycogen Storage Disease; Type IV

GM1 Gangliosidosis

GM2 Gangliosidosis Type II (Burmese Type)

GM2 Gangliosidosis Type II

GM2 Gangliosidosis Type II (Japanese Domestic Type)

GM2 Gangliosidosis Type II (Korat Type)

Hemophilia B Variant 1 and Variant 2

Hyperlipoproteinemia

Hypertrophic Cardiomyopathy (Maine Coon Type)

Hypertrophic Cardiomyopathy (Ragdoll Type)

Hypertrophic Cardiomyopathy (Sphynx Type Risk Factor)

Hypogonadotropic Hypogonadism

Hypokalemic Periodic Paralysis

Hypotrichosis With Short Life Expectancy

Inflammatory Linear Verrucous Epidermal Nevus

L-2-Hydroxyglutaric Aciduria

Methemoglobinemia Variant 1 and Variant 2

Mucolipidosis II

Mucopolysaccharidosis Type I, Type VI (Modifier), Type VI (Siamese Type), Type VII Varient 1, Variant 2.

Multiple Drug Resistance

Myotonia Congenita

Neuronal Ceroid Lipofuscinosis 6, 7 Variant 1, and Variant 2

Niemann-Pick C1 Disease, Variant 1, Variant 2

Niemann-Pick C2 Disease

Oculocutaneous Albinism

Polycystic Kidney Disease, (Siberian Type)

Primary Congenital Glaucoma

Primary Hyperoxaluria Type II

Progressive Retinal Atrophy (PRA)

Pyruvate Kinase Deficiency

Rod-Cone Dysplasia

Spinal Muscular Atrophy

Vitamin D- Dependent Rickets Type IB, Type IA, Variant 1, Type IA Variant 2.