Cat Disease Screening

What you get

Screening across multiple heritable disease markers
Status per condition: Clear / Carrier / At-risk
Care guidance based on results
At-home collection + expert result explanation

How it works

Book via LINE OA

Message GENOPAWS on LINE OA @genopaws to consult and choose the DNA package that suits your pet.

At-home sample collection

Within Bangkok metro, the GENOPAWS team visits your home to collect the sample — convenient, safe, and stress-free.

Expert result explanation

When results return from the lab, our specialist team explains every finding clearly and in detail.

Every package includes at-home sample collection (Bangkok area) and a result explanation by our specialist team.

What we screen for

We screen hundreds of genetic markers and report those relevant to your pet's breed — informational screening, not a diagnosis.

Genetic diseases screened (77)

Acute Intermittent Porphyria (Variant 1)
Acute Intermittent Porphyria (Variant 2)
Acute Intermittent Porphyria (Variant 3)
Acute Intermittent Porphyria (Variant 4) (Siamese Type 1)
Acute Intermittent Porphyria (Variant 5) (Siamese Type 2)
Acute Intermittent Porphyria (Variant 6)
Alpha Mannisidosis (Persian/Domestic Type)
Autoimmune Lymphoproliferative Syndrome
Chylomicronemia - Lipoprotein Lipase Deficiency (Domestic Type)
Congenital Adrenal Hyperplasia
Congenital Erythropoietic Porphyria, Variant 1 (Feline)
Congenital Erythropoietic Porphyria, Variant 2 (Feline)
Congenital Hypothyroidism (Feline)
Congenital Myasthenic Syndrome
Cystinuria, Type 1A (Feline)
Cystinuria, Type B, Variant 1 (Feline)
Cystinuria, Type B, Variant 2 (Feline)
Cystinuria, Type B, Variant 3 (Feline)
Cystinuria, Type B, Variant 4 (Feline)
Cystinuria, Type B, Variant 5 (Feline)
Dihydropyrimidinase Deficiency (Feline)
Epidermolysis Bullosa Simplex (Feline)
Factor XII Deficiency, Variant 1 (Feline)
Factor XII Deficiency, Variant 2 (Feline)
Factor XII Deficiency, Variant 3 (Feline)
Feline Leukocyte Adhesion Deficiency, Type 1 (Feline)
Feline Spongy Encephalopathy (Feline)
Folded Ears with Osteochondrodysplasia (Feline)
Forebrain Commissural Malformation (Feline)
Frontonasal Dysplasia (Burmese Head Defect)
Gangliosidosis GM1 (Japanese Domestic Type)
Gangliosidosis GM2A (Feline)
Glycogen Storage Disease Type IV (Norwegian Forest Cat Type)
GM1 - Gangliosidosis
GM2 Gangliosidosis (Burmese Type)
GM2 Gangliosidosis (Korat Type)
GM2 Gangliosidosis, Type II
Haemophilia B (Variant 1)
Haemophilia B (Variant 2)
Hyperoxaluria GRHPR (Domestic Short/Long Hair Type)
Hypertrophic Cardiomyopathy - Maine Coon
Hypertrophic Cardiomyopathy - Ragdoll
Hypertrophic Cardiomyopathy (Sphynx Type Risk Factor) (Feline)
Hypogonadotropic Hypogonadism (Feline)
Hypokalaemia Periodic Polymyopathy - Burmese
Hypotrichosis with Short Life Expectancy (Feline)
Inflammatory Linear Verrucous Epidermal Nevus (Feline)
L-2-Hydroxyglutaric Aciduria (Feline)
Methemoglobinemia, Variant 1 (Feline)
Methemoglobinemia, Variant 2 (Feline)
Mucolipidosis II (Feline)
Mucopolysaccharidosis Type I
Mucopolysaccharidosis Type VI (Siamese Type)
Mucopolysaccharidosis Type VII, Variant 1 (Feline)
Mucopolysaccharidosis Type VII, Variant 2 (Feline)
Multiple Drug Resistance (Feline)
Myotonia Congenita (Feline)
Neuronal Ceroid Lipofuscinosis 6 (Feline)
Neuronal Ceroid Lipofuscinosis 7, Variant 1 (Feline)
Neuronal Ceroid Lipofuscinosis 7, Variant 2 (Feline)
Niemann-Pick C1 Disease, Variant 1 (Feline)
Niemann-Pick C1 Disease, Variant 2 (Feline)
Niemann-Pick C2 Disease (Feline)
Niemann-Pick Disease - Sphingomyelinosis
Oculocutaneous Albinism (Feline)
Polycystic Kidney Disease
Polycystic Kidney Disease (Siberian Type)
Primary Congenital Glaucoma (Feline)
Progressive Retinal Atrophy (Abyssinian Type)
Progressive Retinal Atrophy (Bengal Type)
Progressive Retinal Atrophy (Persian Type)
Pyruvate Kinase Deficiency (Feline)
Rod-Cone Dysplasia (Feline)
Spinal Muscular Atrophy
Vitamin D-Dependent Rickets Type IB (Feline)
Vitamin D-dependent Rickets, Type IA, Variant 1 (Feline)
Vitamin D-dependent Rickets, Type IA, Variant 2 (Feline)

Cat Disease Screening

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