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.

Behavioral

Canine Compulsive Disorder (CCD)

Blood

Factor VII Deficiency

Haemophilia A, or Factor VIII Deficiency

Haemophilia B, or Factor IX Deficiency

Macrothrombocytopenia

May-Hegglin Anomaly

Polycythemia

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

Thrombopathia

Trapped Neutrophil Syndrome (TNS)

von Willebrand Disease, type 1

von Willebrand Disease, type 2

von Willebrand Disease, type 3

Cancer

Hemangiosarcoma

Histiocytic Sarcoma

Lymphoma

Malignant Melanoma

Mammary Tumors

Mast Cell Tumors

Squamous Cell Carcinoma of the Digit (SCCD)

Connective Tissue

Musladin-Lueke Syndrome

Dental

Amelogenesis Imperfecta

Dental Hypomineralization

Digestive

Inflammatory Bowel Disease (IBD)

Endocrine

Hypothyroidism

Pancreatic Acinar Atrophy (PAA)

Ears

Adult-onset Deafness

Deafness

Eyes

Achromatopsia-2

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

Liver

Gallbladder Mucoceles

Metabolism

Glycogen Storage Disease Ia

Glycogen Storage Disease IIIa

Glycogen Storage Disease VII

Hypocatalasia

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

Muscular

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

Megaesophagus

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

Fucosidosis

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

L-2-hydroxyglutaricacidemia

Lagotto Storage Disease (LSD)

Leukoencephalomyelopathy (LEMP)

Narcolepsy

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

Polyneuropathy 1 (LPN1, or ILPN)

Polyneuropathy 2 (LPN2)

Sensory Neuropathy

Tremors, or Shaking Pup (SHP)

Pharmacology

Multiple Drug Resistance 1 (MDR1)

Poor Metabolizer of Cognitive Enhancer AC-3933

Response to Beta Blocker in Heart Failure

Reproductive

Cryptorchidism

Persistent Mullerian Duct Syndrome

Respiratory

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

Skeletal

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)

Osteoarthritis

Osteochondrodysplasia

Osteochondromatosis

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)

Skin

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)

Ichthyosis

Lethal Acrodermatitis (LAD)

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

Symmetrical Onychomadesis

Other

Embryonic Lethality