Health Screening

We offer the most comprehensive health screening on the market using the most up to date canine science available.  Our full health panel (included in our Health and Behavior Analysis Kit and Breed, Behavior, and Health Plus Kit) covers 322 genetic markers associated with 183 health conditions. Our smaller panel (included in our Breed, Behavior, and Health Analysis Kit) covers 75 genetic markers associated with 32 of the most common canine health conditions. Below is a list of all of the health conditions included in our full health panel. Conditions in black are also included in our smaller health panel.


Canine Compulsive Disorder (CCD)


Factor VII Deficiency

Haemophilia A, or Factor VIII Deficiency

Haemophilia B, or Factor IX Deficiency


May-Hegglin Anomaly


Postoperative hemorrhage, or Platelet Disorder of Swiss Mountain Dog (P2Y12 Receptor Platelet Disorder)

Prekallikrein Deficiency

Pyruvate Kinase Deficiency of Erythrocyte (PK Deficiency)

Scott Syndrome (CSS)

Thrombasthenia, or Glanzmann Thrombasthenia


Trapped Neutrophil Syndrome (TNS)

von Willebrand Disease, type 1

von Willebrand Disease, type 2

von Willebrand Disease, type 3



Histiocytic Sarcoma


Malignant Melanoma

Mammary Tumors

Mast Cell Tumors

Squamous Cell Carcinoma of the Digit (SCCD)

Connective Tissue

Musladin-Lueke Syndrome


Amelogenesis Imperfecta

Dental Hypomineralization


Inflammatory Bowel Disease (IBD)



Pancreatic Acinar Atrophy (PAA)


Adult-onset Deafness




Autosomal-Dominant Progressive Retinal Atrophy (ADPRA)

Bardet-Biedl Syndrome 4

Collie Eye Anomaly

Cone Degeneration (cd), or Achromatopsia

Cone-rod Dystrophy 1 (crd1)

Cone-rod Dystrophy 2 (crd2)

Cone-rod Dystrophy, Standard Wire-Haired Dachshund (CRD^SWHD)

Degenerative myelopathy

Early Retinal Degeneration (erd)

Multifocal Retinopathy 1 (cmr1)

Multifocal Retinopathy 2 (cmr2)

Primary Closed Angle Glaucoma (PCAG)

Primary Hereditary Cataract (PHC)- Early Onset

Primary Lens Luxation (PLL)

Primary open angle glaucoma (POAG)

Progressive Retinal Atrophy (PRA)

Progressive Retinal Atrophy (PRA), type 3

Golden Retriever Progressive Retinal Atrophy, Type 1

Golden Retriever Progressive Retinal Atrophy, Type 2

Rod-cone Dysplasia 1 (rcd1)

Rod-cone Dysplasia 2 (rcd2)

Rod-cone Dysplasia 3 (rcd3)

Rod-cone Dysplasia 4 (rcd4)

Heart/ Circulatory System

Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)

Coronary Artery Disease

Cyclic Neutropenia (CN)

Dilated Cardiomyopathy (DCM)

Long QT Syndrome

Portosystemic Vascular Anomalies (PSVA)

Immune System

Autoinflammatory Disease (AID)

Histiocytosis, Malignant

IgA Deficiency

IgE Response to Dust Mites

Leukocyte Adhesion Deficiency, Type I (LAD1)

Leukocyte Adhesion Deficiency, Type III (LAD3)

Periodic Fever Syndrome

Primary Ciliary Dyskinesia (PCD)

Severe Combined Immunodeficiency Disease (SCID)

Kidneys/ Urinary

Cystinuria, Type IA

Cystinuria, Type IIA

Cystinuria, Type IIB

Hyperuricosuria and Hyperuricemia (huu)

Nephritis, or Alport Syndrome

Polycystic Kidney Disease (PKD)

Primary Hyperoxaluria Type I, or Oxalosis I


Gallbladder Mucoceles


Glycogen Storage Disease Ia

Glycogen Storage Disease IIIa

Glycogen Storage Disease VII


Imerslund-Gräsbeck Syndrome (I-GS), or Selective Cobalamin Malabsorption; Megaloblastic Anemia 1 (MGA1)

Mucopolysaccharidosis I (MPS I)

Mucopolysaccharidosis VI (MPS VI)

Mucopolysaccharidosis VII (MPS VII)

Pyruvate Dehydrogenase Deficiency

Wilson Disease, COMMD1 Type


Centronuclear Myopathy (CNM)

Congenital Myasthenic Syndrome (CMS)

Exercise-Induced Metabolic Myopathy

Exercise-Induced Collapse (EIC) Syndrome

Inherited Myopathy of Great Danes (IMGD)

Limb-girdle Muscular Dystrophy (LGMD)- Type 2F


Muscle Type Phosphofructokinase (M-PFK) Deficiency

Muscular Dystrophy, Duchenne Type, or Golden Retriever Muscular Dystrophy (GRMD)

Muscular Dystrophy, Limb-Girdle, Type 2F (LGMD2F)

Muscular Dystrophy, Ullrich type

Myotubular Myopathy 1, or X-linked Myotubular Myopathy (XLMTM)

Nemaline Myopathy

Nervous System

Acral Mutilation Syndrome

Bandera's Neonatal Ataxia (BNAt)

Canine Hereditary Ataxia

Ataxia, SEL1L-related

Spinocerebellar Ataxia (SCAIS)

Spongy Degeneration with Cerebellar Ataxia 1 (SDCA1)

Spongy Degeneration with Cerebellar Ataxia 2 (SDCA2)

Benign Familial Juvenile Epilepsy, or Remitting Focal Epilepsy

Cerebellar Cortical Degeneration


Gangliosidosis, GM1

Gangliosidosis, GM2, Type I (B variant), or Tay-Sachs Disease

Gangliosidosis, GM2, type II (Sandhoff or variant 0)

Hyperekplexia, or Startle Disease

Hypomyelination of the Central Nervous System

Idiopathic Epilepsy

Krabbe Disease, or Globoid Cell Leukodystrophy


Lagotto Storage Disease (LSD)

Leukoencephalomyelopathy (LEMP)


Necrotising Encephalopathy, or Alaskan Husky Encephalopathy (AHE)

Necrotizing Meningoencephalitis

Neonatal Cerebellar Cortical Degeneration

Neuroaxonal Dystrophy

Neuronal Ceroid Lipofuscinosis, Type 1

Neuronal Ceroid Lipofuscinosis, Type 2

Neuronal Ceroid Lipofuscinosis, Type 4A

Neuronal Ceroid Lipofuscinosis, Type 5

Neuronal Ceroid Lipofuscinosis, Type 6

Neuronal Ceroid Lipofuscinosis, Type 7

Neuronal Ceroid Lipofuscinosis, Type 8

Neuronal Ceroid Lipofuscinosis, Type 10

Neuronal Ceroid Lipofuscinosis, Type 12

Paroxysmal Dyskinesias (PxD)


Polyneuropathy 1 (LPN1, or ILPN)

Polyneuropathy 2 (LPN2)

Sensory Neuropathy

Tremors, or Shaking Pup (SHP)


Multiple Drug Resistance 1 (MDR1)

Poor Metabolizer of Cognitive Enhancer AC-3933

Response to Beta Blocker in Heart Failure



Persistent Mullerian Duct Syndrome


Respiratory Distress Syndrome, or Acute Respiratory Distress Syndrome (ARDS)


Chiari-like Malformation

Chondrodysplasia (defect)

Intervertebral Disc Disease, Type I (IVDD1)

Craniomandibular Osteopathy (CMO), or Caffey Disease

Elbow Dysplasia

Hip Dysplasia

Oculoskeletal Dysplasia 1 (osd1)

Oculoskeletal Dysplasia 2 (osd2)




Osteogenesis Imperfecta

Osteogenesis Imperfecta, Type III

Pituitary Dwarfism, LHX3-related

Skeletal Dysplasia (sd)

Spinal Dysraphism

Spondylocostal Dysostosis (SCD)

Van den Ende-Gupta Syndrome

Vitamin D-deficiency Rickets, Type II (HVDRR)


Anal Furunculosis

Atopic Dermatitis (cAD)

Cleft Lip with or without Cleft Palate (CL/P)

Cleft Palate 1 (CP1)

Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis (CKSID)

Dermatomyositis (DMS)

Ectodermal Dysplasia/Skin Fragility Syndrome (ED-SFS)

Epidermolysis Bullosa

Epidermolytic Hyperkeratosis

Exfoliative Cutaneous Lupus Erythematosus, chr5-related

Hereditary Nasal Parakeratosis (HNPK)


Lethal Acrodermatitis (LAD)

Palmoplantar Keratoderma, or Focal Non-Epidermolytic Palmoplantar Keratoderma (FNEPPK)

Symmetrical Onychomadesis


Embryonic Lethality

We Offer 4 Different Test, Choose Which Kit Is Best For You

What's your Mutt DNA Full Breed Test
What's your Mutt DNA Breed Behavior and Health PLUS1
What's your Mutt DNA Breed Behavior and Health2
What's your Mutt DNA Health and Behavior Kit